Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs371344688
rs371344688
NTRK1
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE Our results indicate that a causative role for M379I and R577G NTRK1 mutations in melanoma development is highly unlikely. 24965840

2014