Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs2839350 0.827 0.080 21 46597307 downstream gene variant G/A snv 0.22 5
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs7452939 0.882 0.080 6 132572626 downstream gene variant G/A snv 4
rs2137947
LOC105376934
0.882 0.040 3 4989276 downstream gene variant C/T snv 0.64 3
rs1334489 0.925 0.040 6 118318224 downstream gene variant T/A snv 0.37 2
rs2295814
EGR2
0.925 0.040 10 62811516 downstream gene variant G/A snv 5.3E-02 2
rs55648125 0.925 0.040 6 50849005 downstream gene variant A/G snv 7.9E-02 2
rs968847 0.925 0.040 10 114998320 downstream gene variant G/T snv 0.20 2
rs116927879 1.000 0.040 7 45825128 downstream gene variant G/A snv 0.21 1
rs11709009 1.000 0.040 3 42473630 downstream gene variant G/A;C snv 1
rs12563333
LINC02779
1.000 0.040 1 220484892 downstream gene variant C/T snv 3.7E-02 1
rs13411201 1.000 0.040 2 60680195 downstream gene variant C/A snv 0.17 1
rs1553656 1.000 0.040 3 36818214 downstream gene variant T/A;C snv 1
rs6130764 1.000 0.040 20 45121769 downstream gene variant T/C snv 0.42 1
rs7544145
LOC105371433
1.000 0.040 1 150166501 downstream gene variant T/C snv 0.25 1
rs78295376 1.000 0.040 4 75570281 downstream gene variant T/C snv 0.11 1
rs8067817 1.000 0.040 17 40007683 downstream gene variant C/G;T snv 1
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5