Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs190121281 19 19141970 upstream gene variant G/A snv 3.5E-03 1
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02 2
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs312985 2 21155933 regulatory region variant A/G snv 0.75 2
rs331
LPL
8 19962894 intron variant G/A snv 0.30 4
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
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
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 7
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
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
rs67418890 1 161571067 intron variant T/A;C snv 1
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15 2
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs7228085
LOC105372112
18 49634444 intergenic variant A/G snv 0.53 1