Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2074560
rs2074560
MX2
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE The Asian haplotype carries a susceptibility allele for melanoma; the European haplotype is tagged by rs2074560, an intronic variant. 24930137

2014