rs11613352, R3HDM2

N. diseases: 9
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.
High density lipoprotein measurement
1440 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.800 1.000 4 2010 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.800 1.000 4 2010 2018
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.700 1.000 2 2010 2013
Gout
CUI: C0018099
Disease: Gout
2354 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.700 1.000 2 2010 2013
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.700 1.000 2 2010 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.010 1.000 1 2015 2015
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.010 1.000 1 2018 2018