rs11554290, NRAS

N. diseases: 59
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.720 GeneticVariation BEFREE These data indicate the reliability of IHC to identify N-RAS Q61R mutated thyroid neoplasia and suggest to adopt this approach for a more accurate management of patients, when indicated. 28064410 2017
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.720 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.720 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.720 GeneticVariation BEFREE In conclusion, NRAS(Q61R) IHC is a highly sensitive and specific tool that is useful for differentiating follicular-patterned thyroid tumors. 26980032 2016