Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 5
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 5
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 4
rs7499892
CETP
16 56972678 intron variant C/G;T snv 4
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 4
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 3
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 3