rs7137828, ATXN2

N. diseases: 15
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.
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 2 2017 2018
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 2 2017 2019
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Diastolic blood pressure measurement
81 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
236 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2016 2016
Juvenile pauciarticular chronic arthritis
31 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Juvenile-Onset Still Disease
CUI: C0087031
Disease: Juvenile-Onset Still Disease
41 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Oligoarticular Juvenile Idiopathic Arthritis
35 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
31 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Rheumatoid Arthritis, Systemic Juvenile
42 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Systemic onset juvenile chronic arthritis
53 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Exfoliation Syndrome
CUI: C0206368
Disease: Exfoliation Syndrome
74 0.763 0.200 12 111494996 intron variant C/A;T snv 0.010 1.000 1 2019 2019