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.
Ovarian Carcinoma
CUI: C0029925
Disease: Ovarian Carcinoma
316 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2010 2010
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
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2016 2016
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
364 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2015 2015
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
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
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
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2015 2015
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
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
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
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
223 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 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
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
665 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2008 2008
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
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
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
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
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
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
341 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012