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.
Acute monoblastic leukemia
CUI: C0457334
Disease: Acute monoblastic leukemia
5 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Adult Acute Monoblastic Leukemia
CUI: C0279629
Disease: Adult Acute Monoblastic Leukemia
5 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Adult Pilocytic Astrocytoma
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
10 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Arthrogryposis
CUI: C0003886
Disease: Arthrogryposis
33 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Childhood Acute Monoblastic Leukemia
5 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
Ductal Carcinoma
CUI: C1176475
Disease: Ductal Carcinoma
11 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2016 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
Juberg-Marsidi syndrome
CUI: C0796003
Disease: Juberg-Marsidi syndrome
14 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
leukemia
CUI: C0023418
Disease: leukemia
144 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
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
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
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Neuromuscular Diseases
CUI: C0027868
Disease: Neuromuscular Diseases
50 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
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
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
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Pilocytic Astrocytoma
CUI: C0334583
Disease: Pilocytic Astrocytoma
14 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007