rs1378942, CSK

N. diseases: 16
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 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 5 2009 2018
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 4 2011 2019
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 2 2011 2011
Diastolic blood pressure measurement
81 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 2 2009 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2011 2011
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2019 2019
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
95 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.240 15 74785026 intron variant C/A;T snv 0.050 0.800 5 2012 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.790 0.240 15 74785026 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.790 0.240 15 74785026 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.790 0.240 15 74785026 intron variant C/A;T snv 0.010 1.000 1 2015 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.790 0.240 15 74785026 intron variant C/A;T snv 0.010 1.000 1 2018 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.790 0.240 15 74785026 intron variant C/A;T snv 0.010 1.000 1 2017 2017