rs121913233, HRAS;LRRC56

N. diseases: 21
Source: CURATED ×
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
98 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.730 1.000 1 2014 2017
melanoma
CUI: C0025202
Disease: melanoma
212 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.720 1.000 0 2016 2018
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
25 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 5 2007 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
67 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 4 2012 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
404 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
114 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
183 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
586 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
195 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
220 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6669 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
203 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
316 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
760 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
248 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
182 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
141 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Nevus Sebaceus of Jadassohn
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
7 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 0
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
7 0.627 0.520 11 533874 missense variant T/A;C;G snv 0.700 0