Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.830 1.000 7 2011 2016
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.810 1.000 3 2011 2018
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.810 1.000 2 2009 2012
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
Low density lipoprotein cholesterol measurement
0.800 1.000 12 2008 2019
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
Low density lipoprotein cholesterol measurement
0.800 1.000 11 2008 2019
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 8 2012 2019
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 8 2009 2019
dbSNP: rs660240
rs660240
1 109275216 3 prime UTR variant T/C snv 0.75
Low density lipoprotein cholesterol measurement
0.800 1.000 8 2008 2019
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
Low density lipoprotein cholesterol measurement
0.800 1.000 7 2008 2019
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 7 2010 2019
dbSNP: rs7528419
rs7528419
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23
Low density lipoprotein cholesterol measurement
0.800 1.000 6 2012 2019
dbSNP: rs7528419
rs7528419
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 5 2012 2019
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
High density lipoprotein measurement
0.800 1.000 4 2012 2019
dbSNP: rs6657811
rs6657811
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10
Low density lipoprotein cholesterol measurement
0.800 1.000 4 2008 2019
dbSNP: rs611917
rs611917
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2008 2018
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
High density lipoprotein measurement
0.800 1.000 3 2012 2018
dbSNP: rs660240
rs660240
1 109275216 3 prime UTR variant T/C snv 0.75
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs6657811
rs6657811
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs7528419
rs7528419
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23
High density lipoprotein measurement
0.800 1.000 3 2012 2019
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
High density lipoprotein measurement
0.800 1.000 2 2012 2018
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2009 2016
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.800 1.000 2 2012 2016
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.720 1.000 3 2014 2019
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.710 1.000 3 2018 2018
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 6 2008 2013