rs687621, ABO

N. diseases: 18
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.851 0.240 9 133261662 intron variant G/A;C snv 0.800 1.000 3 2011 2013
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.851 0.240 9 133261662 intron variant G/A;C snv 0.800 1.000 2 2010 2013
Activated Partial Thromboplastin Time measurement
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
44 0.851 0.240 9 133261662 intron variant G/A;C snv 0.800 1.000 1 2012 2012
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
1178 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2016 2016
Factor VIII measurement
CUI: C2825857
Disease: Factor VIII measurement
42 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2019 2019
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2011 2011
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
1158 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2013 2013
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.851 0.240 9 133261662 intron variant G/A;C snv 0.010 1.000 1 2019 2019