Gene: NRAS ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913237
rs121913237
NRAS
G 0.700 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913250
rs121913250
NRAS
A 0.700 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913250
rs121913250
NRAS
T 0.700 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913250
rs121913250
NRAS
G 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs11554290
rs11554290
NRAS
C 0.700 CausalMutation CLINVAR PIK3CA mutations frequently coexist with RAS and BRAF mutations in patients with advanced cancers. 21829508

2011
dbSNP: rs121913237
rs121913237
NRAS
A 0.700 CausalMutation CLINVAR PIK3CA mutations frequently coexist with RAS and BRAF mutations in patients with advanced cancers. 21829508

2011
dbSNP: rs121913237
rs121913237
NRAS
T 0.700 CausalMutation CLINVAR PIK3CA mutations frequently coexist with RAS and BRAF mutations in patients with advanced cancers. 21829508

2011
dbSNP: rs121913237
rs121913237
NRAS
G 0.700 CausalMutation CLINVAR PIK3CA mutations frequently coexist with RAS and BRAF mutations in patients with advanced cancers. 21829508

2011
dbSNP: rs121913250
rs121913250
NRAS
T 0.700 CausalMutation CLINVAR PIK3CA mutations frequently coexist with RAS and BRAF mutations in patients with advanced cancers. 21829508

2011
dbSNP: rs121913250
rs121913250
NRAS
A 0.700 CausalMutation CLINVAR PIK3CA mutations frequently coexist with RAS and BRAF mutations in patients with advanced cancers. 21829508

2011
dbSNP: rs11554290
rs11554290
NRAS
C 0.700 CausalMutation CLINVAR NRAS mutations are rare in colorectal cancer. 20736745

2010
dbSNP: rs121913237
rs121913237
NRAS
A 0.700 CausalMutation CLINVAR NRAS mutations are rare in colorectal cancer. 20736745

2010
dbSNP: rs121913237
rs121913237
NRAS
T 0.700 CausalMutation CLINVAR NRAS mutations are rare in colorectal cancer. 20736745

2010
dbSNP: rs121913237
rs121913237
NRAS
G 0.700 CausalMutation CLINVAR NRAS mutations are rare in colorectal cancer. 20736745

2010
dbSNP: rs121913250
rs121913250
NRAS
T 0.700 CausalMutation CLINVAR NRAS mutations are rare in colorectal cancer. 20736745

2010
dbSNP: rs121913250
rs121913250
NRAS
A 0.700 CausalMutation CLINVAR NRAS mutations are rare in colorectal cancer. 20736745

2010
dbSNP: rs11554290
rs11554290
NRAS
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs11554290
rs11554290
NRAS
C 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs11554290
rs11554290
NRAS
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121434595
rs121434595
NRAS
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121434596
rs121434596
NRAS
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121434596
rs121434596
NRAS
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913237
rs121913237
NRAS
G 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913237
rs121913237
NRAS
T 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913237
rs121913237
NRAS
A 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016