KLHL38
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
8124658210rs16898671CTrs168986710.000076StrokeHPOID:0001297DOID:6713T,Ccds-synonGWASdb_trait
8124660447rs4871402ACrs48714022.05E-04Common variable immunodeficiencyHPOID:0002721DOID:12177CintronGWASdb_trait