Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs11155372
UTRN
0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs116609693
ANKRD19P
0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2