NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11554290
rs11554290
0.583 0.600 1 114713908 missense variant T/A;C;G snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.020 1.000 2 2018 2019
dbSNP: rs1057519695
rs1057519695
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1057519834
rs1057519834
0.658 0.480 1 114713908 missense variant TG/CT mnv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs121913237
rs121913237
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs121913254
rs121913254
0.658 0.440 1 114713909 stop gained G/A;C;T snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019