Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs312985 2 21155933 regulatory region variant A/G snv 0.75 2
rs190121281 19 19141970 upstream gene variant G/A snv 3.5E-03 1
rs67418890 1 161571067 intron variant T/A;C snv 1
rs72669744 1 55650832 intron variant C/T snv 2.8E-02 1
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs115136538
ADAMTS3
4 72456848 intron variant T/C snv 5.7E-03 1
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38 1
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 4
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12