Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs771306418
CAMK1 ; OGG1
0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs2296972
HTR2A-AS1 ; HTR2A
0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs11060369
TMEM132D
1.000 0.040 12 129475652 intron variant A/C snv 0.41 1
rs8076112
TLCD2
1.000 0.040 17 1708905 intron variant A/C;G snv 0.15 1
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs1800857
CCKAR
0.851 0.120 4 26489489 splice region variant A/G snv 0.17 0.18 4
rs173365
MAPT-AS1 ; LINC02210-CRHR1 ; CRHR1
0.882 0.080 17 45823708 intron variant A/G snv 0.55 3
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs10415555
PEPD
1.000 0.040 19 33519283 intron variant A/G snv 0.19 1
rs10879357
TPH2
1.000 0.040 12 72020783 intron variant A/G snv 0.59 1
rs12061304
LOC107985174
1.000 0.040 1 110695063 intergenic variant A/G snv 0.30 1
rs191260602
GLRB
1.000 0.040 4 157140489 intron variant A/G snv 7.7E-03 1
rs3742278
HTR2A
1.000 0.040 13 46845442 intron variant A/G snv 0.19 1
rs4583306
SLC6A4
1.000 0.040 17 30211697 intron variant A/G snv 0.37 1
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs1418688 1.000 0.040 6 71169166 downstream gene variant A/G;T snv 1
rs4804833
MAP2K7
1.000 0.040 19 7905750 intron variant A/G;T snv 1
rs4977831
FOCAD
1.000 0.040 9 20713069 intron variant A/G;T snv 1
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs1326656542
LIG4
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs11179000
TPH2
0.925 0.040 12 71944848 intron variant A/T snv 0.31 2
rs10801152
LOC105371665
1.000 0.040 1 192792174 intron variant A/T snv 0.31 1