Source: CURATED

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: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
High density lipoprotein measurement
0.800 1.000 10 2009 2019
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 6 2009 2013
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 6 2012 2019
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 5 2009 2018
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
High density lipoprotein measurement
0.800 1.000 5 2008 2019
dbSNP: rs261291
rs261291
1.000 0.080 15 58387979 intron variant T/A;C snv
High density lipoprotein measurement
0.700 1.000 5 2015 2019
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2010 2019
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2018
dbSNP: rs16940212
rs16940212
1.000 0.040 15 58401821 intron variant G/A;T snv
High density lipoprotein measurement
0.800 1.000 3 2011 2019
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2012 2019
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
High density lipoprotein measurement
0.800 1.000 3 2012 2019
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2008 2012
dbSNP: rs261291
rs261291
1.000 0.080 15 58387979 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2018
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2018
dbSNP: rs473224
rs473224
15 58445142 intron variant T/A;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2009 2012
dbSNP: rs588136
rs588136
15 58438299 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2012 2013
dbSNP: rs588136
rs588136
15 58438299 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2012 2017
dbSNP: rs588136
rs588136
15 58438299 intron variant C/G;T snv
High density lipoprotein measurement
0.800 1.000 2 2012 2013
dbSNP: rs10152355
rs10152355
15 58378979 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11632618
rs11632618
15 58432507 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11632618
rs11632618
15 58432507 intron variant G/A;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11632618
rs11632618
15 58432507 intron variant G/A;T snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs11635486
rs11635486
15 58068926 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11856159
rs11856159
15 58406811 intron variant C/A;G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009