Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 5
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02 2
rs1168029
DOCK7
1 62503731 intron variant G/A;C snv 1
rs17610395
CPT1A
11 68794860 missense variant C/G;T snv 1
rs186183604
RAD9A ; LOC100130987
11 67361262 intron variant G/A;T snv 1
rs67418890 1 161571067 intron variant T/A;C snv 1
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 4
rs190121281 19 19141970 upstream gene variant G/A snv 3.5E-03 1
rs181807530
MINK1
17 4871519 intron variant C/G snv 4.8E-03 1
rs115136538
ADAMTS3
4 72456848 intron variant T/C snv 5.7E-03 1
rs72669744 1 55650832 intron variant C/T snv 2.8E-02 1
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 4
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7