Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs1473473
TPH2
0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 4
rs10858583
LOC107984478
1.000 0.040 12 87334666 intergenic variant C/T snv 0.79 3
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs7180942
NTRK3
15 88131345 intron variant T/C snv 0.56 1
rs12475512 2 231433365 downstream gene variant G/A snv 0.47 2
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1805576
FXR1
1.000 0.040 3 180949777 intron variant C/G;T snv 0.24 3
rs4869317
LNPEP
1.000 0.040 5 96956300 intron variant T/A snv 0.22 2
rs13086738
SOX2-OT
1.000 0.040 3 181080939 intron variant A/G snv 0.21 3
rs13077017
FLNB
3 58120049 intron variant C/T snv 0.21 2
rs4854912
SOX2-OT
1.000 0.040 3 181063312 intron variant C/T snv 0.15 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs74566133 8 133766099 regulatory region variant C/T snv 2.6E-02 2
rs138206701
RASGRF2
5 81110747 intron variant A/G snv 1.7E-02 2
rs61754648
HDAC4
2 239090026 missense variant C/T snv 1.4E-03 1.8E-03 1
rs554073050
CCK
0.925 0.040 3 42263460 synonymous variant G/A snv 1.2E-05 7.0E-06 3