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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: 5-70951971-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=70951971&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 70951971,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_000344.4",
"consequences": [
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.865T>A",
"hgvs_p": "p.Cys289Ser",
"transcript": "NM_000344.4",
"protein_id": "NP_000335.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 294,
"cds_start": 865,
"cds_end": null,
"cds_length": 885,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000380707.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000344.4"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.865T>A",
"hgvs_p": "p.Cys289Ser",
"transcript": "ENST00000380707.9",
"protein_id": "ENSP00000370083.4",
"transcript_support_level": 1,
"aa_start": 289,
"aa_end": null,
"aa_length": 294,
"cds_start": 865,
"cds_end": null,
"cds_length": 885,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000344.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380707.9"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.865T>A",
"hgvs_p": "p.Cys289Ser",
"transcript": "ENST00000351205.8",
"protein_id": "ENSP00000305857.5",
"transcript_support_level": 1,
"aa_start": 289,
"aa_end": null,
"aa_length": 294,
"cds_start": 865,
"cds_end": null,
"cds_length": 885,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000351205.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.835-468T>A",
"hgvs_p": null,
"transcript": "ENST00000506163.5",
"protein_id": "ENSP00000424926.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 282,
"cds_start": null,
"cds_end": null,
"cds_length": 849,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000506163.5"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.865T>A",
"hgvs_p": "p.Cys289Ser",
"transcript": "ENST00000932553.1",
"protein_id": "ENSP00000602612.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 294,
"cds_start": 865,
"cds_end": null,
"cds_length": 885,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932553.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.853T>A",
"hgvs_p": "p.Cys285Ser",
"transcript": "ENST00000932554.1",
"protein_id": "ENSP00000602613.1",
"transcript_support_level": null,
"aa_start": 285,
"aa_end": null,
"aa_length": 290,
"cds_start": 853,
"cds_end": null,
"cds_length": 873,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932554.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.793T>A",
"hgvs_p": "p.Cys265Ser",
"transcript": "ENST00000932548.1",
"protein_id": "ENSP00000602607.1",
"transcript_support_level": null,
"aa_start": 265,
"aa_end": null,
"aa_length": 270,
"cds_start": 793,
"cds_end": null,
"cds_length": 813,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932548.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.781T>A",
"hgvs_p": "p.Cys261Ser",
"transcript": "ENST00000932555.1",
"protein_id": "ENSP00000602614.1",
"transcript_support_level": null,
"aa_start": 261,
"aa_end": null,
"aa_length": 266,
"cds_start": 781,
"cds_end": null,
"cds_length": 801,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932555.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.769T>A",
"hgvs_p": "p.Cys257Ser",
"transcript": "NM_022874.2",
"protein_id": "NP_075012.1",
"transcript_support_level": null,
"aa_start": 257,
"aa_end": null,
"aa_length": 262,
"cds_start": 769,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_022874.2"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.769T>A",
"hgvs_p": "p.Cys257Ser",
"transcript": "ENST00000503079.6",
"protein_id": "ENSP00000428128.1",
"transcript_support_level": 5,
"aa_start": 257,
"aa_end": null,
"aa_length": 262,
"cds_start": 769,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000503079.6"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.769T>A",
"hgvs_p": "p.Cys257Ser",
"transcript": "ENST00000870900.1",
"protein_id": "ENSP00000540959.1",
"transcript_support_level": null,
"aa_start": 257,
"aa_end": null,
"aa_length": 262,
"cds_start": 769,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000870900.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.754T>A",
"hgvs_p": "p.Cys252Ser",
"transcript": "ENST00000932551.1",
"protein_id": "ENSP00000602610.1",
"transcript_support_level": null,
"aa_start": 252,
"aa_end": null,
"aa_length": 257,
"cds_start": 754,
"cds_end": null,
"cds_length": 774,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932551.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.712T>A",
"hgvs_p": "p.Cys238Ser",
"transcript": "ENST00000932550.1",
"protein_id": "ENSP00000602609.1",
"transcript_support_level": null,
"aa_start": 238,
"aa_end": null,
"aa_length": 243,
"cds_start": 712,
"cds_end": null,
"cds_length": 732,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932550.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.664T>A",
"hgvs_p": "p.Cys222Ser",
"transcript": "ENST00000514951.5",
"protein_id": "ENSP00000423298.1",
"transcript_support_level": 2,
"aa_start": 222,
"aa_end": null,
"aa_length": 227,
"cds_start": 664,
"cds_end": null,
"cds_length": 684,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000514951.5"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.664T>A",
"hgvs_p": "p.Cys222Ser",
"transcript": "ENST00000932549.1",
"protein_id": "ENSP00000602608.1",
"transcript_support_level": null,
"aa_start": 222,
"aa_end": null,
"aa_length": 227,
"cds_start": 664,
"cds_end": null,
"cds_length": 684,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932549.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.568T>A",
"hgvs_p": "p.Cys190Ser",
"transcript": "ENST00000932552.1",
"protein_id": "ENSP00000602611.1",
"transcript_support_level": null,
"aa_start": 190,
"aa_end": null,
"aa_length": 195,
"cds_start": 568,
"cds_end": null,
"cds_length": 588,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000932552.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.769T>A",
"hgvs_p": "p.Cys257Ser",
"transcript": "XM_047417616.1",
"protein_id": "XP_047273572.1",
"transcript_support_level": null,
"aa_start": 257,
"aa_end": null,
"aa_length": 262,
"cds_start": 769,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417616.1"
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.664T>A",
"hgvs_p": "p.Cys222Ser",
"transcript": "XM_011543597.2",
"protein_id": "XP_011541899.1",
"transcript_support_level": null,
"aa_start": 222,
"aa_end": null,
"aa_length": 227,
"cds_start": 664,
"cds_end": null,
"cds_length": 684,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011543597.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.835-468T>A",
"hgvs_p": null,
"transcript": "NM_001297715.1",
"protein_id": "NP_001284644.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 282,
"cds_start": null,
"cds_end": null,
"cds_length": 849,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001297715.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.834+5795T>A",
"hgvs_p": null,
"transcript": "XM_047417615.1",
"protein_id": "XP_047273571.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 295,
"cds_start": null,
"cds_end": null,
"cds_length": 888,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417615.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.739-468T>A",
"hgvs_p": null,
"transcript": "XM_017009786.2",
"protein_id": "XP_016865275.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 250,
"cds_start": null,
"cds_end": null,
"cds_length": 753,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017009786.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "c.634-468T>A",
"hgvs_p": null,
"transcript": "XM_047417618.1",
"protein_id": "XP_047273574.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 215,
"cds_start": null,
"cds_end": null,
"cds_length": 648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417618.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "n.119T>A",
"hgvs_p": null,
"transcript": "ENST00000510679.1",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000510679.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"hgvs_c": "n.*59-468T>A",
"hgvs_p": null,
"transcript": "ENST00000506239.6",
"protein_id": "ENSP00000422679.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000506239.6"
}
],
"gene_symbol": "SMN1",
"gene_hgnc_id": 11117,
"dbsnp": "rs187925143",
"frequency_reference_population": 0.00005269076,
"hom_count_reference_population": 1,
"allele_count_reference_population": 85,
"gnomad_exomes_af": 0.0000506481,
"gnomad_genomes_af": 0.0000723094,
"gnomad_exomes_ac": 74,
"gnomad_genomes_ac": 11,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.038628339767456055,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.355,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.0869,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.1,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.056,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -3,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PP2,BP4_Strong",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 4,
"pathogenic_score": 1,
"criteria": [
"PP2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_000344.4",
"gene_symbol": "SMN1",
"hgnc_id": 11117,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.865T>A",
"hgvs_p": "p.Cys289Ser"
}
],
"clinvar_disease": " type II, type IV,Kugelberg-Welander disease,Spinal muscular atrophy,Werdnig-Hoffmann disease,not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"phenotype_combined": "not specified|Werdnig-Hoffmann disease;Spinal muscular atrophy, type IV;Spinal muscular atrophy, type II;Kugelberg-Welander disease",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}