Variant List
This API endpoint handles listing (/variants) and retrieval (/variants/<ID>/) of genetic variants from the database
GET /api/combinations/OLI1784/variants/?format=api
https://olida.ibsquare.be/api/variants/3726/relationships/in_combination?format=api", "related": "https://olida.ibsquare.be/api/variants/3726/combinations/?format=api" } }, "gene_name": { "links": { "self": "https://olida.ibsquare.be/api/variants/3726/relationships/gene_name?format=api", "related": "https://olida.ibsquare.be/api/variants/3726/gene/?format=api" }, "data": { "type": "Gene", "id": "NOD2" } } }, "links": { "self": "https://olida.ibsquare.be/api/variants/3726/?format=api" } }, { "type": "SmallVariant", "id": "3720", "attributes": { "frequencies": { "KGP_genomes_maf": 0.0018, "KGP_genomes_AFR_maf": 0.0, "KGP_genomes_AMR_maf": 0.0029, "KGP_genomes_EAS_maf": 0.0, "KGP_genomes_EUR_maf": 0.007, "KGP_genomes_SAS_maf": 0.0, "gnomad_maf": 0.005245, "gnomad_AFR_maf": 0.0001845, "gnomad_AMR_maf": 0.001561, "gnomad_ASJ_maf": 0.009127, "gnomad_EAS_maf": 0.0, "gnomad_FIN_maf": 0.01626, "gnomad_NFE_maf": 0.006804, "gnomad_OTH_maf": 0.00668, "gnomad_SAS_maf": 9.799e-05, "ESP_AA_maf": null, "ESP_EA_maf": null }, "predictions": { "sift_prediction": "Tolerated", "pp2_hvar_prediction": "Benign", "cadd_prediction": 1.157052, "mutationtaster_prediction": "Disease causing" }, "status": "CU", "genomic_position_hg19": 3293403, "genomic_position_hg38": 3243403, "chromosome": "16", "annotation_flag": null, "lastmodified": "2024-02-29T15:02:34.655139", "ref_allele": "T", "alt_allele": "C", "cdna_change": "c.2084A>G", "protein_change": "p.Lys695Arg", "transcript_id": "NM_000243.3", "dbsnp_id": "NA", "variant_effect": null }, "relationships": { "in_combination": { "meta": { "count": 3 }, "data": [ { "type": "Combination", "id": "OLI1753" }, { "type": "Combination", "id": "OLI1777" }, { "type": "Combination", "id": "OLI1784" } ], "links": { "self": "https://olida.ibsquare.be/api/variants/3720/relationships/in_combination?format=api", "related": "https://olida.ibsquare.be/api/variants/3720/combinations/?format=api" } }, "gene_name": { "links": { "self": "https://olida.ibsquare.be/api/variants/3720/relationships/gene_name?format=api", "related": "https://olida.ibsquare.be/api/variants/3720/gene/?format=api" }, "data": { "type": "Gene", "id": "MEFV" } } }, "links": { "self": "https://olida.ibsquare.be/api/variants/3720/?format=api" } }, { "type": "SmallVariant", "id": "3739", "attributes": { "frequencies": { "KGP_genomes_maf": 0.006, "KGP_genomes_AFR_maf": 0.0015, "KGP_genomes_AMR_maf": 0.013, "KGP_genomes_EAS_maf": 0.0, "KGP_genomes_EUR_maf": 0.0189, "KGP_genomes_SAS_maf": 0.0, "gnomad_maf": 0.01318, "gnomad_AFR_maf": 0.003077, "gnomad_AMR_maf": 0.009022, "gnomad_ASJ_maf": 0.01766, "gnomad_EAS_maf": 0.0, "gnomad_FIN_maf": 0.01128, "gnomad_NFE_maf": 0.02029, "gnomad_OTH_maf": 0.01808, "gnomad_SAS_maf": 0.003627, "ESP_AA_maf": null, "ESP_EA_maf": null }, "predictions": { "sift_prediction": "Tolerated", "pp2_hvar_prediction": "Unknown", "cadd_prediction": 0.685628, "mutationtaster_prediction": "Disease causing" }, "status": "CU", "genomic_position_hg19": 6442643, "genomic_position_hg38": 6333477, "chromosome": "12", "annotation_flag": null, "lastmodified": "2024-02-29T15:02:35.994051", "ref_allele": "C", "alt_allele": "T", "cdna_change": "c.362G>A", "protein_change": "p.Arg121Gln", "transcript_id": "NM_001065.4", "dbsnp_id": "NA", "variant_effect": null }, "relationships": { "in_combination": { "meta": { "count": 7 }, "data": [ { "type": "Combination", "id": "OLI1773" }, { "type": "Combination", "id": "OLI1774" }, { "type": "Combination", "id": "OLI1775" }, { "type": "Combination", "id": "OLI1783" }, { "type": "Combination", "id": "OLI1784" }, { "type": "Combination", "id": "OLI1785" }, { "type": "Combination", "id": "OLI1788" } ], "links": { "self": "https://olida.ibsquare.be/api/variants/3739/relationships/in_combination?format=api", "related": "https://olida.ibsquare.be/api/variants/3739/combinations/?format=api" } }, "gene_name": { "links": { "self": "https://olida.ibsquare.be/api/variants/3739/relationships/gene_name?format=api", "related": "https://olida.ibsquare.be/api/variants/3739/gene/?format=api" }, "data": { "type": "Gene", "id": "TNFRSF1A" } } }, "links": { "self": "https://olida.ibsquare.be/api/variants/3739/?format=api" } } ], "meta": { "database_name": "OLIgogenic diseases DAtabase (OLIDA)", "resource_url": "olida.ibsquare.be", "api_release_year": "2021", "api_developer": [ [ "Arnau Dillen", "arnau.dillen@ulb.ac.be" ], [ "Charlotte Nachtegael", "charlotte.nachtegael@ulb.be" ] ], "api_version": "0.3", "api_maintainers": [ [ "Charlotte Nachtegael", "charlotte.nachtegael@ulb.be" ] ], "api_documentation": [ "olida.ibsquare.be/api/swagger", "olida.ibsquare.be/api/redoc" ], "copyright": "Copyright (c) 2025 · OLIDA All Rights Reserved.", "license": "CC Attribution-NonCommercial 4.0 International License", "ontologies": { "ORDO": "http://bioportal.bioontology.org/ontologies/ORDO", "GENO": "http://purl.obolibrary.org/obo/geno.owl", "MI": "http://purl.obolibrary.org/obo/mi.owl", "NCIT": "http://purl.obolibrary.org/obo/ncit.owl", "OGI": "http://purl.obolibrary.org/obo/ogi.owl", "OGG": "http://purl.obolibrary.org/obo/ogg.owl" }, "relevant_publications_doi": [ "10.1093/nar/gkv1068", "10.1093/database/baac023" ], "Variant serializers": [ "SmallVariantSerializer", "CopyNumberVariantSerializer" ], "size": 3 } }{ "data": [ { "type": "SmallVariant", "id": "3726", "attributes": { "frequencies": { "KGP_genomes_maf": 0.0333, "KGP_genomes_AFR_maf": 0.0023, "KGP_genomes_AMR_maf": 0.0634, "KGP_genomes_EAS_maf": 0.0, "KGP_genomes_EUR_maf": 0.1054, "KGP_genomes_SAS_maf": 0.0143, "gnomad_maf": 0.06269, "gnomad_AFR_maf": 0.01409, "gnomad_AMR_maf": 0.05098, "gnomad_ASJ_maf": 0.1713, "gnomad_EAS_maf": 0.0006525, "gnomad_FIN_maf": 0.03934, "gnomad_NFE_maf": 0.08848, "gnomad_OTH_maf": 0.07918, "gnomad_SAS_maf": 0.02062, "ESP_AA_maf": null, "ESP_EA_maf": null }, "predictions": { "sift_prediction": "Deleterious", "pp2_hvar_prediction": "Benign", "cadd_prediction": 0.151927, "mutationtaster_prediction": "Polymorphism" }, "status": "CU", "genomic_position_hg19": 50757276, "genomic_position_hg38": 50723365, "chromosome": "16", "annotation_flag": null, "lastmodified": "2024-02-29T15:02:34.949154", "ref_allele": "G", "alt_allele": "A", "cdna_change": "c.2863G>A", "protein_change": "p.Val955Ile", "transcript_id": "NM_022162.3", "dbsnp_id": "NA", "variant_effect": null }, "relationships": { "in_combination": { "meta": { "count": 8 }, "data": [ { "type": "Combination", "id": "OLI1757" }, { "type": "Combination", "id": "OLI1758" }, { "type": "Combination", "id": "OLI1771" }, { "type": "Combination", "id": "OLI1772" }, { "type": "Combination", "id": "OLI1777" }, { "type": "Combination", "id": "OLI1778" }, { "type": "Combination", "id": "OLI1779" }, { "type": "Combination", "id": "OLI1784" } ], "links": { "self": "