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: rs16891982
rs16891982
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0037290
Disease:
Skin Pigmentation 		0.800 GeneticVariation GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
dbSNP: rs16891982
rs16891982
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0037290
Disease:
Skin Pigmentation 		G 0.800 GeneticVariation GWASCAT Identification of a novel locus associated with skin colour in African-admixed populations. 28300201 2017
dbSNP: rs16891982
rs16891982
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0037290
Disease:
Skin Pigmentation 		C 0.800 GeneticVariation GWASCAT A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007
dbSNP: rs16891982
rs16891982
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0037290
Disease:
Skin Pigmentation 		C 0.800 GeneticVariation GWASDB A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007