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
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
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
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
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
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
rs242924
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.882 0.080 17 45808001 intron variant G/T snv 0.44 3
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs11179000
TPH2
0.925 0.040 12 71944848 intron variant A/T snv 0.31 2
rs11724320
NPY5R ; NPY1R
0.925 0.040 4 163346771 intron variant T/C snv 0.56 2
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs4076452
LINC02210-CRHR1
1.000 0.040 17 45778528 intron variant G/C snv 0.16 2
rs4760820
TPH2
0.925 0.040 12 72003216 intron variant C/G snv 0.29 2
rs10415555
PEPD
1.000 0.040 19 33519283 intron variant A/G snv 0.19 1