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 Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.700 1.000 1 2018 2018
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
56 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.020 1.000 2 2009 2020
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.020 1.000 2 2010 2012
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.020 1.000 2 2005 2007
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
55 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.020 1.000 2 2009 2020
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2005 2005
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2015 2015
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2010 2010
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2010 2010
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2005 2005
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2012 2012
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2009 2009
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2008 2008
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
81 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2005 2005
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2010 2010
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2005 2005
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1.000 1 2008 2008
Stage 0 Gallbladder Cancer AJCC v8
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
56 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014
Stage IIA Gallbladder Cancer AJCC v8
CUI: C4525300
Disease: Stage IIA Gallbladder Cancer AJCC v8
56 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014
Stage IIB Gallbladder Cancer AJCC v8
CUI: C4525301
Disease: Stage IIB Gallbladder Cancer AJCC v8
56 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014
Stage III Gallbladder Cancer AJCC v8
CUI: C4525302
Disease: Stage III Gallbladder Cancer AJCC v8
56 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014
Stage IV Gallbladder Cancer AJCC v8
CUI: C4525305
Disease: Stage IV Gallbladder Cancer AJCC v8
56 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 0.010 1 2014 2014