Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1477692170
rs1477692170
POMC
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		0.010 GeneticVariation BEFREE K36E attenuated α-MSH induced cAMP pathways, contributing to hypopigmentation. 28114924

2017