Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
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
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs6782011
GRM7
0.807 0.120 3 7457960 intron variant C/T snv 0.52 7
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs908867 0.851 0.160 11 27724217 intron variant C/G;T 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
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs1997679
DTNBP1
0.882 0.120 6 15658674 intron variant G/A snv 0.35 6
rs41279104
NOS1
0.827 0.160 12 117439680 intron variant C/T snv 0.11 6
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 6
rs1867283
NTRK2
0.925 0.080 9 84835851 intron variant G/A snv 0.39 5
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 5