Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066844
rs2066844
NOD2
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE There were no statistically significant differences between prevalence of G908R and R702W in malignant melanoma patients and controls. 15785318

2005