NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Disease: Noonan Syndrome 6 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606921
rs267606921
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C2750732
Disease:
Noonan Syndrome 6 		0.800 GeneticVariation UNIPROT A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803 2010
dbSNP: rs267606921
rs267606921
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C2750732
Disease:
Noonan Syndrome 6 		0.800 GeneticVariation UNIPROT Noonan syndrome: clinical features, diagnosis, and management guidelines. 20876176 2010
dbSNP: rs267606921
rs267606921
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C2750732
Disease:
Noonan Syndrome 6 		A 0.800 CausalMutation CLINVAR