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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
223 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.700 1 2012 2012
Blood pressure finding
CUI: C1271104
Disease: Blood pressure finding
223 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.700 1 2012 2012
Systemic arterial pressure
CUI: C1272641
Disease: Systemic arterial pressure
223 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.700 1 2012 2012
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.070 1.000 7 2008 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.060 1.000 6 2010 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.050 1.000 5 2009 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.050 1.000 5 2009 2015
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2012 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2010 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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
409 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2010 2012
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
400 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2010 2012
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1878 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.020 1.000 2 2012 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
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
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
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
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
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
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
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
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2012 2012