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.
Primary central nervous system lymphoma
3 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2011 2011
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
4 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2013 2013
Anterior encephalocele
CUI: C4024948
Disease: Anterior encephalocele
5 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2018 2018
Renal sclerosis with hypertension
CUI: C0264657
Disease: Renal sclerosis with hypertension
6 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Myeloid Leukemia
CUI: C0023470
Disease: Myeloid Leukemia
6 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2014 2014
Congenital omphalocele
CUI: C0795690
Disease: Congenital omphalocele
6 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
9 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2018 2018
AIDS related complex
CUI: C0001857
Disease: AIDS related complex
10 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2016 2016
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
15 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Cognitive changes
CUI: C1392786
Disease: Cognitive changes
16 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
17 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2013 2013
Liver and Intrahepatic Biliary Tract Carcinoma
18 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2014 2014
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
26 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2013 2013
Experimental Organism Basal Cell Carcinoma
33 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
34 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2015 2015
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
37 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2014 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
60 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
64 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2014 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
66 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
71 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2014 2014
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
93 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Childhood Acute Lymphoblastic Leukemia
97 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2016 2018
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
99 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2013 2018
Overweight
CUI: C0497406
Disease: Overweight
126 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2015 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
209 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2015 2015