Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs7224199
SLC6A4
0.827 0.160 17 30196708 3 prime UTR variant G/T snv 0.49 7
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs5177
LRP8
0.851 0.120 1 53246063 3 prime UTR variant G/A;C snv 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5