Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2
rs55945116
SEC11A
0.882 0.040 15 84676882 intron variant G/C snv 0.26 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs853679
ZSCAN31
0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs5743467
DEFB1
0.925 0.040 8 6874007 intron variant C/G snv 0.19 3
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 1
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs2221540
OPCML
0.925 0.040 11 132846474 intron variant A/G snv 0.11 2
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs2302045
MTERF4 ; SNED1
0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3