ZFAND6
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1580377452rs6495474GTrs64954745.24E-05Type 2 diabetesHPOID:0005978DOID:9352TintronGWASdb_trait
1580377452rs6495474GTrs64954741.11E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
1580392689rs10519280AGrs105192803.23E-04Lung function (forced vital capacity)HPOID:0002088DOID:850AintronGWASdb_trait
1580401973rs12438497ATrs124384971.15E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
1580413384rs2903265AGrs29032659.15E-05Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
1580413384rs2903265AGrs29032659.60E-06Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
1580413384rs2903265AGrs29032659.57E-06Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1580414718rs11635107ACrs116351078.92E-05Cognitive performanceHPOID:0100543DOID:1561AintronGWASdb_trait
1580414718rs11635107ACrs116351072.69E-04Lung function (forced vital capacity)HPOID:0002088DOID:850AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000086666.18 ZFAND6 610183