Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs62100776
DCC
0.925 0.040 18 53228263 intron variant A/T snv 0.35 2
rs200855945
SSPN ; BHLHE41
0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs853679
ZSCAN31
0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs56388524 0.925 0.040 5 45757459 intergenic variant C/A;T snv 2.0E-02 3
rs5743467
DEFB1
0.925 0.040 8 6874007 intron variant C/G snv 0.19 3
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs17790731
RFESD
0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-02 4
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs55679149
LOC105378841
0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2