rs121913233, HRAS;LRRC56

N. diseases: 37
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Dysplastic Nevus
CUI: C0205748
Disease: Dysplastic Nevus
7 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Eccrine porocarcinoma
CUI: C1266065
Disease: Eccrine porocarcinoma
11 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2018 2018
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Follicular Variant Thyroid Gland Papillary Carcinoma
CUI: C3714651
Disease: Follicular Variant Thyroid Gland Papillary Carcinoma
13 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2013 2013
Inverted urothelial papilloma
CUI: C1334282
Disease: Inverted urothelial papilloma
3 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Paraganglioma
CUI: C0030421
Disease: Paraganglioma
36 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Recurrent tumor
CUI: C0521158
Disease: Recurrent tumor
33 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Skin Carcinogenesis
CUI: C1519346
Disease: Skin Carcinogenesis
7 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2012 2012
Solid/Multicystic Ameloblastoma
CUI: C1513734
Disease: Solid/Multicystic Ameloblastoma
10 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Trichilemmoma
CUI: C0334263
Disease: Trichilemmoma
4 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014