Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 3
rs115485095
CYP21A2 ; EHMT2
6 31888293 intron variant G/A snv 3
rs115845232
LOC112267902 ; HLA-B
6 31304484 intron variant C/T snv 3
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv 3
rs116477171
CYP21A2 ; C2
6 31918153 intron variant C/G;T snv 3
rs11652146
ZNF652
17 49345001 intron variant G/A;C snv 4
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 3
rs11987974
LOC105379376
8 36966299 intergenic variant C/A;T snv 4
rs12047226
DOCK7
1 62639867 intron variant T/A;C snv 3
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 3
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1495743 8 18415790 intergenic variant G/A;C snv 4
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs150641967
HAPLN4
19 19259532 intron variant AGAC/-;AGACAGAC delins 4
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 3
rs1558861 11 116736721 regulatory region variant C/G;T snv 4
rs1565228
BDNF-AS
11 27564889 intron variant G/A;C snv 4
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 4
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3