rs727503094, LRRC56;HRAS

N. diseases: 41
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 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1 1999 1999
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.100 1.000 13 2010 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.020 1.000 2 2006 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.020 1.000 2 2006 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2016 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2015 2015
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2006 2006
melanoma
CUI: C0025202
Disease: melanoma
515 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.040 1.000 4 2011 2015
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2019 2019
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2019 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2011 2011
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2011 2011
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2011 2011
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.020 1.000 2 2015 2017
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2015 2015
leukemia
CUI: C0023418
Disease: leukemia
144 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2014 2014
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2011 2011
Neuromuscular Diseases
CUI: C0027868
Disease: Neuromuscular Diseases
50 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017
Arthrogryposis
CUI: C0003886
Disease: Arthrogryposis
33 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 0.010 1.000 1 2017 2017