Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11340914
TCEA3
1 23421504 intron variant AA/-;A;AAA delins 0.65 2
rs12130333 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 2
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 2
rs13399758
CAD
2 27232858 intron variant T/C snv 0.20 2
rs28927680
BUD13
11 116748357 3 prime UTR variant C/G;T snv 2
rs3927680 9 16887368 intergenic variant T/A snv 0.43 2
rs7157785
SYNE2
14 63768838 intron variant G/T snv 0.24 2
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 3
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
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 3
rs118146573
CETP
16 56967026 intron variant G/A snv 9.4E-02 3
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 3
rs12047226
DOCK7
1 62639867 intron variant T/A;C snv 3
rs12208357
SLC22A1
1.000 0.080 6 160122116 missense variant C/T snv 5.2E-02 4.9E-02 3
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 3
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 3
rs12721054
APOC1
19 44919330 3 prime UTR variant A/G snv 3.7E-02 3
rs13329672
ALDH1A2
15 58407738 intron variant C/T snv 0.31 3
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 3