rs104894226, HRAS;LRRC56

N. diseases: 19
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.
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
10 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2005 2005
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
37 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.010 1.000 1 2007 2007
Thymoma
CUI: C0040100
Disease: Thymoma
17 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.710 1.000 3 2010 2015
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
226 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 2 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
121 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
228 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
203 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
223 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
149 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
303 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
228 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
72 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Squamous cell carcinoma of the head and neck
288 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Transitional cell carcinoma of bladder
147 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
19 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.810 1.000 3 2005 2017