Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 4
rs312985 2 21155933 regulatory region variant A/G snv 0.75 2
rs7228085
LOC105372112
18 49634444 intergenic variant A/G snv 0.53 1
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs11075253
PDXDC1 ; NTAN1
16 15054789 intron variant C/A snv 0.22 1
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs181807530
MINK1
17 4871519 intron variant C/G snv 4.8E-03 1
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02 2
rs17610395
CPT1A
11 68794860 missense variant C/G;T snv 1
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 4
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 4
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15 1
rs72669744 1 55650832 intron variant C/T snv 2.8E-02 1