Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 5
rs74617384
LPA
0.925 0.080 6 160576086 intron variant A/G;T snv 5
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 4
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 4
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 4
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 4
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 4
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs11601507
TRIM5
1.000 0.040 11 5679844 missense variant C/A;T snv 9.3E-02; 4.0E-06 3
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 3
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 3
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 3
rs2880301
TPTE2
1.000 0.040 13 19526394 intron variant C/T snv 3
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 3
rs3936510
C5orf67
1.000 0.040 5 56565039 intron variant G/A;T snv 3