SLC10A2, solute carrier family 10 member 2, 6555

N. diseases: 66; N. variants: 9
Disease: Bile Acid Malabsorption, Primary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917848
rs121917848
Entrez Id: 6555
Gene Symbol: SLC10A2
SLC10A2
CUI: C2750087
Disease:
Bile Acid Malabsorption, Primary 		0.700 GeneticVariation UNIPROT Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2). 9109432 1997