Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519734
rs1057519734
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1
CUI: C0025202
Disease:
melanoma
T 0.700 CausalMutation CLINVAR Melanoma genome sequencing reveals frequent PREX2 mutations. 22622578 2012
dbSNP: rs1057519734
rs1057519734
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1
CUI: C0025202
Disease:
melanoma
T 0.700 CausalMutation CLINVAR Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma. 22197931 2011