SLC45A2, solute carrier family 45 member 2, 51151

N. diseases: 75; N. variants: 46
Disease: Skin Pigmentation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASCAT Identification of a novel locus associated with skin colour in African-admixed populations. 28300201 2017
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASCAT Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. 25963972 2015
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASCAT A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASDB A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007