RXRG, retinoid X receptor gamma, 6258

N. diseases: 40; N. variants: 9
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 AlteredExpression disease BEFREE Mutation screening and association of human retinoid X receptor gamma variation with lipid levels in familial type 2 diabetes. 12175776 2002