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: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.810 1.000 1 2012 2012
dbSNP: rs11823543
rs11823543
11 116778419 3 prime UTR variant G/A snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2011 2011
dbSNP: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs6589566
rs6589566
0.882 0.080 11 116781707 intron variant G/A;C;T snv
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2008 2008
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1142098
Disease: Vitamin E Assay
Vitamin E Assay
0.800 1.000 1 2011 2011
dbSNP: rs121917821
rs121917821
0.925 0.080 11 116790814 stop gained G/A snv 4.0E-06
CUI: C0020481
Disease: Hyperlipoproteinemia Type V
Hyperlipoproteinemia Type V
0.710 1.000 1 2005 2005
dbSNP: rs10750096
rs10750096
11 116786072 intron variant C/A snv 0.92
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs113932726
rs113932726
11 116779922 intron variant C/T snv 9.8E-03
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs11604424
rs11604424
11 116780399 intron variant C/G;T snv
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs11604424
rs11604424
11 116780399 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11823543
rs11823543
11 116778419 3 prime UTR variant G/A snv 0.11
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11823543
rs11823543
11 116778419 3 prime UTR variant G/A snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12285095
rs12285095
11 116787315 non coding transcript exon variant T/G snv 9.8E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs12285095
rs12285095
11 116787315 non coding transcript exon variant T/G snv 9.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12285095
rs12285095
11 116787315 non coding transcript exon variant T/G snv 9.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs12285095
rs12285095
11 116787315 non coding transcript exon variant T/G snv 9.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012