Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs56131196
APOC1
0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 5
rs2030746
LOC105373585
0.925 0.120 2 120551912 downstream gene variant C/T snv 0.44 5
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs1277930
PSRC1
1 109279521 downstream gene variant G/A snv 0.63 4
rs314253
DLG4
17 7188331 downstream gene variant T/C snv 0.37 4
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs11577931 1 109278262 downstream gene variant A/G snv 5.5E-02 3
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3