Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs186183604
RAD9A ; LOC100130987
11 67361262 intron variant G/A;T snv 1
rs190121281 19 19141970 upstream gene variant G/A snv 3.5E-03 1
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38 1
rs67418890 1 161571067 intron variant T/A;C snv 1
rs7228085
LOC105372112
18 49634444 intergenic variant A/G snv 0.53 1
rs72669744 1 55650832 intron variant C/T snv 2.8E-02 1
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 5
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 7
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
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
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
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
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
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26