SLC10A1, solute carrier family 10 member 1, 6554

N. diseases: 54; N. variants: 7
Disease: Vitamin D Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2296651
rs2296651
Entrez Id: 6554
Gene Symbol: SLC10A1
SLC10A1
CUI: C0042870
Disease:
Vitamin D Deficiency 		0.010 GeneticVariation BEFREE Individuals with homozygous p.Ser267Phe in SLC10A1 are prone to vitamin D deficiency, deviated sex hormones and blood lipids. 28835676 2017