rs1748195, DOCK7

N. diseases: 8
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.851 0.120 1 62583922 intron variant C/G;T snv 0.800 1.000 4 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.851 0.120 1 62583922 intron variant C/G;T snv 0.800 1.000 3 2012 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.851 0.120 1 62583922 intron variant C/G;T snv 0.700 1.000 2 2018 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.851 0.120 1 62583922 intron variant C/G;T snv 0.700 1.000 1 2015 2015
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.120 1 62583922 intron variant C/G;T snv 0.700 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.851 0.120 1 62583922 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.120 1 62583922 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.851 0.120 1 62583922 intron variant C/G;T snv 0.010 1.000 1 2018 2018