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: rs10889353
rs10889353
1 62652525 intron variant A/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2009 2019
dbSNP: rs10128711
rs10128711
11 18611437 intron variant T/C snv 0.64 0.55
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs11136341
rs11136341
8 143969375 intron variant A/G snv 0.40
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs11220462
rs11220462
11 126374057 intron variant G/A snv 0.12
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs11563251
rs11563251
2 233770738 3 prime UTR variant C/T snv 0.19
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2013
dbSNP: rs12027135
rs12027135
1 25449242 intron variant A/T snv 0.50
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs1564348
rs1564348
6 160157828 intron variant T/C snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2019
dbSNP: rs2131925
rs2131925
1 62560271 intron variant G/T snv 0.57
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2019
dbSNP: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2019
dbSNP: rs2277862
rs2277862
20 35564866 non coding transcript exon variant C/T snv 0.18 0.17
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs2290159
rs2290159
3 12587421 non coding transcript exon variant G/C snv 0.23
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2013
dbSNP: rs2642442
rs2642442
1 220800221 intron variant C/T snv 0.73
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs2814982
rs2814982
6 34578783 upstream gene variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs2902940
rs2902940
20 40462847 regulatory region variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2013
dbSNP: rs3757354
rs3757354
6 16127176 upstream gene variant C/T snv 0.27
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs514230
rs514230
1 234722850 upstream gene variant A/T snv 0.62
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs581080
rs581080
9 15305380 intron variant G/C snv 0.72
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2017
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: rs6029526
rs6029526
20 41043978 intron variant T/A snv 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs7206971
rs7206971
17 47347749 intron variant G/A;T snv 0.47
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs7241918
rs7241918
18 49634583 intergenic variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs7499892
rs7499892
16 56972678 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs7515577
rs7515577
1 92543881 intron variant C/A;G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2018
dbSNP: rs7941030
rs7941030
11 122651667 upstream gene variant T/C snv 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2010 2013