Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs10454453
PDE4B
1.000 0.040 1 66206849 intron variant C/A snv 0.48 1
rs1487275
TPH2
1.000 0.040 12 72016512 intron variant C/A snv 0.71 1
rs4145262 1.000 0.040 12 105659532 regulatory region variant C/A snv 4.8E-02 1
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs75634836
HTR2A
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs9302001
LOC101927284
1.000 0.040 13 94811138 intergenic variant C/A;T snv 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs4760820
TPH2
0.925 0.040 12 72003216 intron variant C/G snv 0.29 2
rs2770292
HTR2A
1.000 0.040 13 46860971 intron variant C/G snv 0.18 1
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs754635
CCK
1.000 0.040 3 42263639 splice region variant C/G;T snv 0.84; 5.6E-06 3
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs13356494 1.000 0.040 5 135991866 regulatory region variant C/G;T snv 1
rs37790 1.000 0.040 5 53346682 intergenic variant C/G;T snv 1
rs860554
PKP1
1.000 0.040 1 201293304 intron variant C/G;T snv 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
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
rs140701
SLC6A4
0.790 0.200 17 30211514 intron variant C/T snv 0.40 7