Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519702
rs1057519702
KIT
CUI: C0025202
Disease: melanoma
melanoma 		C 0.700 CausalMutation CLINVAR Genetic aberrations in primary esophageal melanomas: molecular analysis of c-KIT, PDGFR, KRAS, NRAS and BRAF in a series of 10 cases. 21131919

2011