SKAP2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
726726320rs212853AGrs2128531.20E-05Urinary metabolitesHPOID:0000079DOID:557AintronGWASdb_trait
726729740rs17291131GArs172911319.53E-04Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
726764618rs10227898CTrs102278981.70E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
726774325rs4722631GArs47226311.60E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
726789814rs11770043GArs117700431.40E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
726793064rs11773029CTrs117730291.00E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
726793515rs12700761GArs127007611.30E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
726804018rs17372780GCrs173727801.60E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
726814394rs7807640TCrs78076401.20E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
726816648rs1123158AGrs11231581.20E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
726853934rs3823934TCrs38239344.76E-04Lung function (forced vital capacity)HPOID:0002088DOID:850AintronGWASdb_trait
726891665rs7804356TCrs78043565.00E-09Type 1 diabetesHPOID:0100651DOID:9744TintronGWASdb_trait
726891665rs7804356TCrs78043565.30E-09Multiple sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:2377TintronGWASdb_trait
726892440rs10486483GArs104864833.00E-08Crohn's diseaseHPOID:0100280DOID:8778AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000005020.12 SKAP2 605215