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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 7-2572244-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=2572244&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 2572244,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "NM_152558.5",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.312T>C",
          "hgvs_p": "p.Thr104Thr",
          "transcript": "NM_152558.5",
          "protein_id": "NP_689771.3",
          "transcript_support_level": null,
          "aa_start": 104,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": 312,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 515,
          "cdna_end": null,
          "cdna_length": 6857,
          "mane_select": "ENST00000402050.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.312T>C",
          "hgvs_p": "p.Thr104Thr",
          "transcript": "ENST00000402050.7",
          "protein_id": "ENSP00000385597.2",
          "transcript_support_level": 1,
          "aa_start": 104,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": 312,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 515,
          "cdna_end": null,
          "cdna_length": 6857,
          "mane_select": "NM_152558.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
          "hgvs_p": "p.Thr39Thr",
          "transcript": "ENST00000623361.3",
          "protein_id": "ENSP00000485601.1",
          "transcript_support_level": 1,
          "aa_start": 39,
          "aa_end": null,
          "aa_length": 630,
          "cds_start": 117,
          "cds_end": null,
          "cds_length": 1893,
          "cdna_start": 428,
          "cdna_end": null,
          "cdna_length": 6775,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "n.*89T>C",
          "hgvs_p": null,
          "transcript": "ENST00000325997.13",
          "protein_id": "ENSP00000314011.10",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2235,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "n.446T>C",
          "hgvs_p": null,
          "transcript": "ENST00000470731.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2251,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "n.*89T>C",
          "hgvs_p": null,
          "transcript": "ENST00000325997.13",
          "protein_id": "ENSP00000314011.10",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2235,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.312T>C",
          "hgvs_p": "p.Thr104Thr",
          "transcript": "NM_001287499.2",
          "protein_id": "NP_001274428.1",
          "transcript_support_level": null,
          "aa_start": 104,
          "aa_end": null,
          "aa_length": 702,
          "cds_start": 312,
          "cds_end": null,
          "cds_length": 2109,
          "cdna_start": 515,
          "cdna_end": null,
          "cdna_length": 2500,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.312T>C",
          "hgvs_p": "p.Thr104Thr",
          "transcript": "ENST00000476665.5",
          "protein_id": "ENSP00000480715.1",
          "transcript_support_level": 2,
          "aa_start": 104,
          "aa_end": null,
          "aa_length": 702,
          "cds_start": 312,
          "cds_end": null,
          "cds_length": 2109,
          "cdna_start": 415,
          "cdna_end": null,
          "cdna_length": 2400,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.264T>C",
          "hgvs_p": "p.Thr88Thr",
          "transcript": "NM_001287500.2",
          "protein_id": "NP_001274429.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 686,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 2061,
          "cdna_start": 467,
          "cdna_end": null,
          "cdna_length": 2452,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.264T>C",
          "hgvs_p": "p.Thr88Thr",
          "transcript": "ENST00000611775.4",
          "protein_id": "ENSP00000480668.1",
          "transcript_support_level": 2,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 686,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 2061,
          "cdna_start": 297,
          "cdna_end": null,
          "cdna_length": 2289,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.264T>C",
          "hgvs_p": "p.Thr88Thr",
          "transcript": "NM_001410865.1",
          "protein_id": "NP_001397794.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 679,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 2040,
          "cdna_start": 467,
          "cdna_end": null,
          "cdna_length": 6809,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.264T>C",
          "hgvs_p": "p.Thr88Thr",
          "transcript": "ENST00000438376.6",
          "protein_id": "ENSP00000396178.2",
          "transcript_support_level": 5,
          "aa_start": 88,
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          "cds_start": 264,
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          "cdna_start": 394,
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          "cdna_length": 2170,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
          "hgvs_p": "p.Thr39Thr",
          "transcript": "NM_001287502.2",
          "protein_id": "NP_001274431.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 637,
          "cds_start": 117,
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          "cdna_start": 421,
          "cdna_end": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 3,
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          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
          "hgvs_p": "p.Thr39Thr",
          "transcript": "NM_001287501.2",
          "protein_id": "NP_001274430.1",
          "transcript_support_level": null,
          "aa_start": 39,
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          "cds_start": 117,
          "cds_end": null,
          "cds_length": 1893,
          "cdna_start": 421,
          "cdna_end": null,
          "cdna_length": 6763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
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          "intron_rank": null,
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          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
          "hgvs_p": "p.Thr39Thr",
          "transcript": "ENST00000325979.11",
          "protein_id": "ENSP00000313772.7",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.312T>C",
          "hgvs_p": "p.Thr104Thr",
          "transcript": "ENST00000415271.6",
          "protein_id": "ENSP00000404643.1",
          "transcript_support_level": 5,
          "aa_start": 104,
          "aa_end": null,
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          "cds_start": 312,
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          "cdna_start": 473,
          "cdna_end": null,
          "cdna_length": 899,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
          "hgvs_p": "p.Thr39Thr",
          "transcript": "ENST00000422276.3",
          "protein_id": "ENSP00000402108.3",
          "transcript_support_level": 5,
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          "cds_length": 384,
          "cdna_start": 274,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
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          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
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          "transcript": "ENST00000423395.5",
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
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          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.333T>C",
          "hgvs_p": "p.Thr111Thr",
          "transcript": "XM_047420081.1",
          "protein_id": "XP_047276037.1",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.333T>C",
          "hgvs_p": "p.Thr111Thr",
          "transcript": "XM_017011902.2",
          "protein_id": "XP_016867391.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 702,
          "cds_start": 333,
          "cds_end": null,
          "cds_length": 2109,
          "cdna_start": 606,
          "cdna_end": null,
          "cdna_length": 6948,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IQCE",
          "gene_hgnc_id": 29171,
          "hgvs_c": "c.117T>C",
          "hgvs_p": "p.Thr39Thr",
          "transcript": "XM_006715676.3",
          "protein_id": "XP_006715739.1",
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      ],
      "gene_symbol": "IQCE",
      "gene_hgnc_id": 29171,
      "dbsnp": "rs2917751",
      "frequency_reference_population": 0.746449,
      "hom_count_reference_population": 452641,
      "allele_count_reference_population": 1204597,
      "gnomad_exomes_af": 0.750096,
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      "gnomad_genomes_ac": 108217,
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      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7799999713897705,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.029999999329447746,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.78,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.22,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.03,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
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      "mitotip_score": null,
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      "acmg_score": -15,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -15,
          "benign_score": 15,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_152558.5",
          "gene_symbol": "IQCE",
          "hgnc_id": 29171,
          "effects": [
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          "inheritance_mode": "AR",
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      "clinvar_disease": " postaxial, type a7,IQCE-related disorder,Polydactyly",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "Polydactyly, postaxial, type a7|IQCE-related disorder",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}