Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs140504
LOC107985554 ; BCR
0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs2199503
GSK3B
0.851 0.080 3 120059642 intron variant T/C snv 0.79 4
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs2919375
NRG1
0.925 0.040 8 32719327 intron variant G/A snv 0.77 3
rs9394309
FKBP5
0.851 0.040 6 35654004 intron variant G/A snv 0.74 4
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 4
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs2137947
LOC105376934
0.882 0.040 3 4989276 downstream gene variant C/T snv 0.64 3
rs2710117
CNTNAP2
0.882 0.040 7 147904680 intron variant T/A snv 0.63 3
rs1690818
CNTN5
0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs12476147
ZNF804A
0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs4236710
NRG1
0.882 0.040 8 32571241 intron variant C/T snv 0.58 3
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4761545 0.925 0.040 12 94032692 regulatory region variant G/T snv 0.56 3
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs6276
DRD2
0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 8
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs35792458
XKR6
0.925 0.040 8 10964921 intron variant G/C snv 0.53 3