Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs11754661
MTHFD1L
0.851 0.120 6 150885942 intron variant G/A;T snv 6
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 4
rs1339039642
MTHFD1L
6 150905744 missense variant C/T snv 1.4E-05 2