Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913250
rs121913250
NRAS
0.710 GeneticVariation BEFREE In the present study, we report 2 patients with somatic mosaicism for oncogenic NRAS mutations (G12D and G12S) associated with the development of JMML. 22753870

2012
dbSNP: rs121913250
rs121913250
NRAS
T 0.710 CausalMutation CLINVAR A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803

2010
dbSNP: rs121913250
rs121913250
NRAS
T 0.710 CausalMutation CLINVAR Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. 19047918

2009
dbSNP: rs121913250
rs121913250
NRAS
T 0.710 CausalMutation CLINVAR Hyperactive Ras in developmental disorders and cancer. 17384584

2007
dbSNP: rs121913250
rs121913250
NRAS
T 0.710 CausalMutation CLINVAR Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies. 16518851

2006
dbSNP: rs121913250
rs121913250
NRAS
T 0.710 CausalMutation CLINVAR Juvenile myelomonocytic leukemia and Noonan syndrome. 10598665

2000