Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3731249
rs3731249
CDKN2A
CUI: C1456781
Disease: Benign melanocytic nevus
Benign melanocytic nevus 		0.010 GeneticVariation BEFREE There was no association between Ala148Thr status and nevus number or history of melanoma, and therefore the results did not support the hypothesis that the Ala148Thr variant is a low penetrance melanoma or nevus susceptibility allele. 12406345

2002