PCGF6
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
10105075712rs12220267CTrs122202671.00E-213Arsenic metabolism and toxicityHPOID:0011013DOID:0050032CintronGWASdb_trait
10105080575rs7093667TCrs70936678.90E-05White matter hyperintensity burdenHPOID:0007103|HPOID:0002637DOID:936|DOID:2316|DOID:3527CintronGWASdb_trait
10105092447rs10883855TCrs108838557.70E-05White matter hyperintensity burdenHPOID:0007103|HPOID:0002637DOID:936|DOID:2316|DOID:3527CintronGWASdb_trait
10105101701rs11191659CTrs111916590.0009Urinary concentrations of arsenic metabolites (percentage monomethylarsonic acid)HPOID:0011013DOID:0050032CintronGWASdb_trait
10105101701rs11191659CTrs111916591.04E-12Arsenic metabolism and toxicityHPOID:0011013DOID:0050032CintronGWASdb_trait
10105101701rs11191659CTrs111916593.29E-12Arsenic metabolism and toxicityHPOID:0011013DOID:0050032CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000156374.14 PCGF6 607816