Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894228
rs104894228
HRAS ; LRRC56
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.710 GeneticVariation BEFREE Using next-generation sequencing techniques, we were able to identify the same HRAS G13R mutation within both components of the tumor, and to show the absence of additional mutated modifier genes in a panel of 300 cancer-related genes. 24628623

2014