NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Disease: Papillary thyroid carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.020 GeneticVariation BEFREE Mutations in RAS genes (HRAS G13R, KRAS G12D, KRAS Q61R, NRAS Q61R) were detected in benign lesions and HRAS Q61R, NRAS Q61K mutations in PTCs. 31085772 2019
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.020 GeneticVariation BEFREE The BRAF T1799A mutation was detected in 10 PTC cases, while two different NRAS mutations in codon 61 (C181A and A182G) were found in 2 PTC cases. 30361901 2018
dbSNP: rs1057519695
rs1057519695
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.010 GeneticVariation BEFREE Mutations in RAS genes (HRAS G13R, KRAS G12D, KRAS Q61R, NRAS Q61R) were detected in benign lesions and HRAS Q61R, NRAS Q61K mutations in PTCs. 31085772 2019
dbSNP: rs1057519834
rs1057519834
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.010 GeneticVariation BEFREE Mutations in RAS genes (HRAS G13R, KRAS G12D, KRAS Q61R, NRAS Q61R) were detected in benign lesions and HRAS Q61R, NRAS Q61K mutations in PTCs. 31085772 2019
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.010 GeneticVariation BEFREE KRAS G12V Mutation in Acquired Resistance to Combined BRAF and MEK Inhibition in Papillary Thyroid Cancer. 31085763 2019
dbSNP: rs121913254
rs121913254
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.010 GeneticVariation BEFREE Mutations in RAS genes (HRAS G13R, KRAS G12D, KRAS Q61R, NRAS Q61R) were detected in benign lesions and HRAS Q61R, NRAS Q61K mutations in PTCs. 31085772 2019