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: rs72547505
rs72547505
Entrez Id: 6555
Gene Symbol: SLC10A2
SLC10A2
CUI: C2750087
Disease:
Bile Acid Malabsorption, Primary 		0.700 GeneticVariation UNIPROT