Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2017 2019
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 2 2017 2018
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
Juvenile pauciarticular chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
Rheumatoid Arthritis, Systemic Juvenile
0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease
0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2016 2016
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
Oligoarticular Juvenile Idiopathic Arthritis
0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
Systemic onset juvenile chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7137828
rs7137828
0.763 0.200 12 111494996 intron variant C/A;T snv
Diastolic blood pressure measurement
0.700 1.000 1 2018 2018