Source: GWASDB ×
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 25
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 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
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 4
rs506585 2 21174310 intergenic variant G/A;C;T snv 3