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
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs12944712
CRHR1 ; LINC02210-CRHR1
0.925 0.040 17 45793781 intron variant G/A snv 0.35 3
rs4819035
ADARB1
21 45225800 3 prime UTR variant T/G snv 0.20 1
rs1456031
FOXP2
7 114656047 intron variant T/C snv 0.44 1