Source: GWASDB

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: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
0.810 1.000 1 2013 2017
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
Low density lipoprotein cholesterol measurement
0.800 1.000 10 2008 2019
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.800 1.000 1 2011 2011
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.720 1.000 2 2011 2016
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 10 2008 2013
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009