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: 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: 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: 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: rs6589566
rs6589566
0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 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: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
High density lipoprotein measurement
0.800 1.000 2 2012 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: rs6589566
rs6589566
0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.710 1.000 2 2014 2018
dbSNP: rs6589566
rs6589566
0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 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: 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
dbSNP: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total 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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
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: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs2075290
rs2075290
0.882 0.160 11 116782580 intron variant C/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2016 2016