rs104894230, HRAS;LRRC56

N. diseases: 73
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2014 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1 1999 1999
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.100 1.000 13 2010 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2006 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2006 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2014 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 3 2014 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.040 1.000 4 2011 2015
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 10 2002 2017
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.710 1.000 2 2011 2016
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016