rs4238833, AFG3L1P

N. diseases: 2
Disease: melanoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
melanoma
CUI: C0025202
Disease: melanoma
0.700 GeneticVariation GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340 2012
melanoma
CUI: C0025202
Disease: melanoma
0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 21926416 2011