SLC4A2, solute carrier family 4 member 2, 6522

N. diseases: 35; N. variants: 6
Disease: Primary biliary cirrhosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3793336
rs3793336
Entrez Id: 6522
Gene Symbol: SLC4A2
SLC4A2
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.010 GeneticVariation BEFREE No associations with disease or liver transplantation were detected, but two variants, rs2303929 and rs3793336, were associated with negativity for antimitochondrial antibodies among the PBC patients. 19491853 2009