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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: 11-73975506-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=73975506&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 73975506,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_003355.3",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "NM_003355.3",
"protein_id": "NP_003346.2",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000663595.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003355.3"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000663595.2",
"protein_id": "ENSP00000499695.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003355.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000663595.2"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000310473.11",
"protein_id": "ENSP00000312029.3",
"transcript_support_level": 1,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000310473.11"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.833G>T",
"hgvs_p": "p.Arg278Leu",
"transcript": "ENST00000880151.1",
"protein_id": "ENSP00000550210.1",
"transcript_support_level": null,
"aa_start": 278,
"aa_end": null,
"aa_length": 320,
"cds_start": 833,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880151.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "NM_001381943.1",
"protein_id": "NP_001368872.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381943.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "NM_001381944.1",
"protein_id": "NP_001368873.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381944.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "NM_001381945.1",
"protein_id": "NP_001368874.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381945.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "NM_001381947.1",
"protein_id": "NP_001368876.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381947.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "NM_001381948.1",
"protein_id": "NP_001368877.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381948.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000880147.1",
"protein_id": "ENSP00000550206.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880147.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000880149.1",
"protein_id": "ENSP00000550208.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880149.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000880150.1",
"protein_id": "ENSP00000550209.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880150.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000880152.1",
"protein_id": "ENSP00000550211.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880152.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000880153.1",
"protein_id": "ENSP00000550212.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880153.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000880154.1",
"protein_id": "ENSP00000550213.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880154.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu",
"transcript": "ENST00000952750.1",
"protein_id": "ENSP00000622809.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 309,
"cds_start": 800,
"cds_end": null,
"cds_length": 930,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952750.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.728G>T",
"hgvs_p": "p.Arg243Leu",
"transcript": "ENST00000952751.1",
"protein_id": "ENSP00000622810.1",
"transcript_support_level": null,
"aa_start": 243,
"aa_end": null,
"aa_length": 285,
"cds_start": 728,
"cds_end": null,
"cds_length": 858,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952751.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.698G>T",
"hgvs_p": "p.Arg233Leu",
"transcript": "NM_001381949.1",
"protein_id": "NP_001368878.1",
"transcript_support_level": null,
"aa_start": 233,
"aa_end": null,
"aa_length": 275,
"cds_start": 698,
"cds_end": null,
"cds_length": 828,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381949.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.659G>T",
"hgvs_p": "p.Arg220Leu",
"transcript": "ENST00000912379.1",
"protein_id": "ENSP00000582438.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 262,
"cds_start": 659,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912379.1"
},
{
"aa_ref": "R",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.605G>T",
"hgvs_p": "p.Arg202Leu",
"transcript": "NM_001381950.1",
"protein_id": "NP_001368879.1",
"transcript_support_level": null,
"aa_start": 202,
"aa_end": null,
"aa_length": 244,
"cds_start": 605,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001381950.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.605G>T",
"hgvs_p": "p.Arg202Leu",
"transcript": "ENST00000880148.1",
"protein_id": "ENSP00000550207.1",
"transcript_support_level": null,
"aa_start": 202,
"aa_end": null,
"aa_length": 244,
"cds_start": 605,
"cds_end": null,
"cds_length": 735,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880148.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "UCP2",
"gene_hgnc_id": 12518,
"hgvs_c": "c.635-385G>T",
"hgvs_p": null,
"transcript": "ENST00000536983.5",
"protein_id": "ENSP00000441147.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 225,
"cds_start": null,
"cds_end": null,
"cds_length": 678,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000536983.5"
},
{
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{
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"downstream_gene_variant"
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"biotype": "protein_coding",
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],
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"dbsnp": "rs753260142",
"frequency_reference_population": 6.8560115e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.85601e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0631551742553711,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.224,
"revel_prediction": "Benign",
"alphamissense_score": 0.1038,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.42,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.262,
"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,
"mitotip_prediction": null,
"acmg_score": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_003355.3",
"gene_symbol": "UCP2",
"hgnc_id": 12518,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.800G>T",
"hgvs_p": "p.Arg267Leu"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}