Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
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
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
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
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
rs11644601
RRN3 ; PDXDC1
16 15078261 intron variant T/C snv 0.21 4
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 4
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 4