Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9875578 3 13752941 intergenic variant G/A;C snv 1
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs9370822
DTNBP1 ; LOC105374947
0.882 0.120 6 15544505 intron variant A/C snv 0.36 7
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs876657421
CBS
0.763 0.240 21 43063074 coding sequence variant -/CCCAGCAAAAGCCCCACCTGGATGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG;CCCAGCAAAAGCCCCACCTGGGTGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG delins 11
rs8192506
DBI
1.000 0.040 2 119372265 missense variant A/C;G snv 4.0E-06; 2.5E-02 2
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs79928194
GIGYF2
2 232784580 intron variant T/C snv 0.14 1
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs774847933
COMT ; MIR4761
0.882 0.200 22 19962797 missense variant A/G snv 8.0E-06 5
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs757281
RAPGEF3
1.000 0.040 12 47748635 non coding transcript exon variant C/A;G;T snv 2
rs7528604
PDE4B
0.925 0.040 1 65941669 intron variant G/A snv 0.42 3
rs75012854
MIR4761 ; COMT
0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs72711240 4 134774652 intron variant C/T snv 2.2E-02 1
rs7209436
LINC02210-CRHR1 ; CRHR1
0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs7194256
SLC6A2
0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 7
rs7124442
BDNF-AS ; BDNF
0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7