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: 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: rs11604424
rs11604424
11 116780399 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs11604424
rs11604424
11 116780399 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs149808404
rs149808404
11 116790406 stop gained G/A;C snv 4.1E-05; 8.1E-06
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.020 1.000 2 2014 2019
dbSNP: rs3741298
rs3741298
11 116786845 intron variant C/T snv 0.73
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
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: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 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: 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: rs17120029
rs17120029
11 116779402 intron variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
11 116791110 missense variant T/C snv 0.89 0.94
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2075294
rs2075294
11 116787406 intron variant G/T snv 3.5E-02
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2019 2019