SLC45A2, solute carrier family 45 member 2, 51151

N. diseases: 75; N. variants: 46
Disease: Skin Pigmentation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs183671
rs183671
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0037290
Disease:
Skin Pigmentation 		T 0.700 GeneticVariation GWASCAT Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. 25963972 2015
dbSNP: rs183671
rs183671
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0037290
Disease:
Skin Pigmentation 		0.700 GeneticVariation GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018