FAF2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5175893063rs2033198GArs20331989.73E-05Cognitive test performanceHPOID:0100543DOID:1561AintronGWASdb_trait
5175893063rs2033198GArs20331985.69E-05Erythrocyte countsHPOID:0001627|HPOID:0001871DOID:74|DOID:114AintronGWASdb_trait
5175898997rs11134975CArs111349757.64E-05Cognitive test performanceHPOID:0100543DOID:1561AintronGWASdb_trait
5175901585rs13154670TCrs131546701.26E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652TintronGWASdb_trait
5175935316rs2963672TCrs29636728.77E-04Multiple complex diseasesHPOID:0000118NATUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000113194.12 FAF2 616935