PIAS2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1844396917rs642897TGrs6428975.00E-07Personality dimensionsHPOID:0012075DOID:1510GUTR-3GWASdb_trait
1844414614rs649076AGrs6490766.30E-07Personality dimensionsHPOID:0012075DOID:1510GintronGWASdb_trait
1844417456rs607780CTrs6077805.80E-07Personality dimensionsHPOID:0012075DOID:1510AintronGWASdb_trait
1844422333rs695001ACrs6950015.40E-07Personality dimensionsHPOID:0012075DOID:1510CintronGWASdb_trait
1844422661rs7236403TCrs72364038.60E-06Central corneal thicknessHPOID:0000501DOID:1067|DOID:10126CintronGWASdb_trait
1844429182rs626217TGrs6262175.30E-07Personality dimensionsHPOID:0012075DOID:1510GintronGWASdb_trait
1844431832rs658756TCrs6587562.55E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1844431832rs658756TCrs6587564.90E-07Personality dimensionsHPOID:0012075DOID:1510GintronGWASdb_trait
1844439011rs2032215ACrs20322154.70E-07Personality dimensionsHPOID:0012075DOID:1510CintronGWASdb_trait
1844442402rs577200TGrs5772001.30E-06Personality dimensionsHPOID:0012075DOID:1510CintronGWASdb_trait
1844444778rs605487GCrs6054875.20E-07Personality dimensionsHPOID:0012075DOID:1510CintronGWASdb_trait
1844455873rs2156050AGrs21560505.30E-07Personality dimensionsHPOID:0012075DOID:1510GintronGWASdb_trait
1844460037rs7240239TCrs72402395.30E-07Personality dimensionsHPOID:0012075DOID:1510CintronGWASdb_trait
1844467368rs4890341TC,Grs48903417.10E-07Personality dimensionsHPOID:0012075DOID:1510CintronGWASdb_trait
1844467515rs8086286GArs80862863.33E-05Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1844475220rs10853545ATrs108535451.73E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
1844475220rs10853545ATrs108535455.40E-07Personality dimensionsHPOID:0012075DOID:1510TintronGWASdb_trait
1844484372rs2051292CGrs20512921.40E-06Personality dimensionsHPOID:0012075DOID:1510GintronGWASdb_trait
1844497724rs4890707CGrs48907073.80E-07Personality dimensionsHPOID:0012075DOID:1510GnearGene-5GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000078043.15 PIAS2 603567