rs505922, ABO

N. diseases: 34
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.
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.689 0.520 9 133273813 intron variant C/T snv 0.740 1.000 6 2009 2018
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.689 0.520 9 133273813 intron variant C/T snv 0.740 1.000 4 2009 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.689 0.520 9 133273813 intron variant C/T snv 0.720 1.000 3 2013 2018
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.689 0.520 9 133273813 intron variant C/T snv 0.800 1.000 3 2009 2012
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.689 0.520 9 133273813 intron variant C/T snv 0.020 2 2013 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.689 0.520 9 133273813 intron variant C/T snv 0.710 1.000 2 2018 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.689 0.520 9 133273813 intron variant C/T snv 0.020 1.000 2 2014 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.689 0.520 9 133273813 intron variant C/T snv 0.020 1.000 2 2014 2015
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.689 0.520 9 133273813 intron variant C/T snv 0.800 1.000 2 2013 2017
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2012 2012
Alkaline phosphatase measurement
CUI: C0201850
Disease: Alkaline phosphatase measurement
79 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2017 2017
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1 2012 2012
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2012 2012
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
28 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1 2013 2013
Duodenal Ulcer
CUI: C0013295
Disease: Duodenal Ulcer
33 0.689 0.520 9 133273813 intron variant C/T snv 0.810 1.000 1 2012 2012
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.689 0.520 9 133273813 intron variant C/T snv 0.800 1.000 1 2013 2013
Homocysteine measurement
CUI: C2242817
Disease: Homocysteine measurement
33 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2017 2017
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2018 2018
Invasive carcinoma of breast
CUI: C0853879
Disease: Invasive carcinoma of breast
21 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2012 2012
Iron deficiency
CUI: C0240066
Disease: Iron deficiency
13 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2018 2018
Malaria
CUI: C0024530
Disease: Malaria
148 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2013 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1 2012 2012
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015