Source: ALL

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: rs201079485
rs201079485
0.925 0.080 11 116790940 stop gained G/A;T snv 8.0E-05; 4.0E-06
CUI: C0813230
Disease: Serum triglycerides increased
Serum triglycerides increased
0.700 0
dbSNP: rs201079485
rs201079485
0.925 0.080 11 116790940 stop gained G/A;T snv 8.0E-05; 4.0E-06
CUI: C0020480
Disease: Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type IV
0.700 0
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs143292359
rs143292359
11 116790285 missense variant G/A snv 5.9E-04 5.0E-04
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.010 < 0.001 1 2008 2008
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
0.010 < 0.001 1 2006 2006
dbSNP: rs3135507
rs3135507
0.925 0.120 11 116790772 missense variant C/T snv 5.0E-02 5.5E-02
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 < 0.001 1 2018 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 22 2009 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
High density lipoprotein measurement
0.800 1.000 12 2009 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 9 2010 2019
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.080 1.000 8 2003 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 7 2011 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.830 1.000 6 2010 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Low density lipoprotein cholesterol measurement
0.800 1.000 6 2010 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 6 2009 2013
dbSNP: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2011 2019
dbSNP: rs603446
rs603446
1.000 0.040 11 116783719 intron variant C/T snv 0.33
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2011 2019
dbSNP: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
High density lipoprotein measurement
0.800 1.000 4 2011 2019
dbSNP: rs35120633
rs35120633
11 116784884 missense variant G/A;C snv 6.6E-02; 8.0E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2009 2019
dbSNP: rs3741298
rs3741298
11 116786845 intron variant C/T snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2012 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 4 2013 2018
dbSNP: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2019
dbSNP: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
High density lipoprotein measurement
0.700 1.000 3 2018 2019
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.720 1.000 3 2008 2019