SLC12A1, solute carrier family 12 member 1, 6557

N. diseases: 87; N. variants: 29
Disease: Skin Pigmentation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12913316
rs12913316
Entrez Id: 6557;399697
Gene Symbol: SLC12A1;CTXN2
SLC12A1;CTXN2
CUI: C0037290
Disease:
Skin Pigmentation 		0.700 GeneticVariation GWASDB A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007