PARD6B
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2049363182rs2064278GTrs20642781.13E-05Cleft lipHPOID:0000202DOID:9296GintronGWASdb_trait
2049363182rs2064278GTrs20642782.79E-05Orofacial cleftsHPOID:0000202DOID:0050567GintronGWASdb_trait
2049367076rs6020721TGrs60207213.06E-04Birth weightHPOID:0004323DOID:783|DOID:9352|DOID:1287TUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000124171.8 PARD6B 608975