Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3813567
CHRNB4
1.000 0.080 15 78642209 intron variant G/A snv 0.77 2
rs4425326
NPY2R
0.925 0.080 4 155186084 intron variant C/T snv 0.47 2
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs4887074
LOC112268142 ; CHRNB4
1.000 0.080 15 78659768 intron variant G/C snv 0.56 2
rs4938056
HTR3B
0.925 0.080 11 113915817 intron variant C/T snv 0.51 2
rs6484320
BDNF-AS ; BDNF
1.000 0.080 11 27681641 intron variant T/A;G snv 2
rs7934165
BDNF
0.925 0.160 11 27710436 intron variant G/A snv 0.49 2
rs910083
DNMT3B
1.000 0.080 20 32790884 intron variant A/C;G;T snv 2
rs921451
DDC
1.000 0.080 7 50555587 intron variant T/C snv 0.32 2
rs963468
DRD3
0.925 0.080 3 114144040 intron variant G/A snv 0.30 2
rs10082479
CHAT
1.000 0.080 10 49621173 intron variant A/T snv 0.23 1
rs10865246
NRXN1
1.000 0.080 2 50443116 intron variant C/A;T snv 1
rs1122530
NTRK2
1.000 0.080 9 84849437 intron variant A/G snv 0.22 1
rs1187272
NTRK2
1.000 0.080 9 84789171 intron variant G/A;C snv 1
rs12266458
CHAT
1.000 0.080 10 49639951 intron variant C/T snv 0.11 1
rs12466358
CHRND
1.000 0.080 2 232532815 intron variant T/G snv 0.22 1
rs13286166
KANK1
1.000 0.080 9 741307 intron variant G/A;T snv 1
rs1331188
SHC3
1.000 0.080 9 89110472 intron variant G/T snv 0.23 1
rs13334632
ZCCHC14
1.000 0.080 16 87457213 intron variant T/C snv 0.16 1
rs1411836
SHC3
1.000 0.080 9 89160966 intron variant C/G;T snv 0.12 1
rs1541333
DBH
1.000 0.080 9 133646263 intron variant C/G snv 0.52 1
rs1547696
SHC3
1.000 0.080 9 89079205 intron variant T/C snv 0.60 1
rs1556384
SHC3
1.000 0.080 9 89149212 intron variant T/C snv 0.93 1
rs1659400
NTRK2
1.000 0.080 9 84711079 intron variant A/G snv 0.60 1
rs16969868
FAM155A
1.000 0.080 13 107219364 intron variant G/C snv 3.8E-02 1