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
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs140701
SLC6A4
0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs771306418
CAMK1 ; OGG1
0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs2296972
HTR2A-AS1 ; HTR2A
0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs173365
MAPT-AS1 ; LINC02210-CRHR1 ; CRHR1
0.882 0.080 17 45823708 intron variant A/G snv 0.55 3