HRAS, HRas proto-oncogene, GTPase, 3265

N. diseases: 698; N. variants: 29
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: rs104894228
rs104894228
0.605 0.560 11 534286 missense variant C/A;G;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.710 1.000 6 2007 2015
dbSNP: rs104894229
rs104894229
0.564 0.600 11 534289 missense variant C/A;G;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.700 1.000 5 2007 2016
dbSNP: rs104894230
rs104894230
0.564 0.600 11 534288 missense variant C/A;G;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.700 1.000 5 2007 2016
dbSNP: rs121913233
rs121913233
0.627 0.520 11 533874 missense variant T/A;C;G snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.700 1.000 5 2007 2016
dbSNP: rs121913496
rs121913496
0.724 0.440 11 533873 missense variant C/A;G;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12628
rs12628
0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013