KRAS, KRAS proto-oncogene, GTPase, 3845

N. diseases: 1213; N. variants: 54
Disease: Noonan Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202247812
rs202247812
Entrez Id: 3845
Gene Symbol: KRAS
KRAS
CUI: C0028326
Disease:
Noonan Syndrome 		0.010 GeneticVariation BEFREE Our findings implicate that N116S change in KRAS is a hyperactive mutation which is a causative agent of NS through maldevelopment of the heart. 22302539 2012