Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs806371
CNR1
0.882 0.040 6 88146644 intron variant T/G snv 0.18 4
rs58532686 1.000 0.040 16 55652905 upstream gene variant CT/- del 5.1E-02 1