Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 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
rs2072621
GPR50-AS1 ; GPR50
0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
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