Disease: Serum total cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17883880
CHUK
10 100230590 intron variant T/A snv 1.2E-02 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs611917
CELSR2
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs6602910
GAS6
13 113846042 intron variant T/A;C snv 0.53 2
rs499790
LINC02702
11 116649022 intron variant C/T snv 8.6E-02 4
rs480823
LINC02702
11 116655013 intron variant T/C snv 7.3E-02 4
rs481843
LINC02702
1.000 0.040 11 116655150 non coding transcript exon variant C/T snv 8.8E-02 4
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 5
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 3
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs28927680
BUD13
11 116748357 3 prime UTR variant C/G;T snv 4
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs12285095
ZPR1
11 116787315 non coding transcript exon variant T/G snv 9.8E-02 4