NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Disease: Noonan Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913250
rs121913250
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0028326
Disease:
Noonan Syndrome 		T 0.700 CausalMutation CLINVAR A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803 2010
dbSNP: rs121913250
rs121913250
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0028326
Disease:
Noonan Syndrome 		T 0.700 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
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0028326
Disease:
Noonan Syndrome 		T 0.700 CausalMutation CLINVAR Hyperactive Ras in developmental disorders and cancer. 17384584 2007
dbSNP: rs121913250
rs121913250
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0028326
Disease:
Noonan Syndrome 		T 0.700 CausalMutation CLINVAR Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies. 16518851 2006
dbSNP: rs121913250
rs121913250
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0028326
Disease:
Noonan Syndrome 		T 0.700 CausalMutation CLINVAR Juvenile myelomonocytic leukemia and Noonan syndrome. 10598665 2000