Disease: Mood Disorders
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
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs2072621
GPR50-AS1 ; GPR50
0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs9370822
DTNBP1 ; LOC105374947
0.882 0.120 6 15544505 intron variant A/C snv 0.36 7
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs1867283
NTRK2
0.925 0.080 9 84835851 intron variant G/A snv 0.39 5