Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12475512 2 231433365 downstream gene variant G/A snv 0.47 2
rs13077017
FLNB
3 58120049 intron variant C/T snv 0.21 2
rs138206701
RASGRF2
5 81110747 intron variant A/G snv 1.7E-02 2
rs7322916
ATP8A2
13 25433839 intron variant G/A;C snv 2
rs74566133 8 133766099 regulatory region variant C/T snv 2.6E-02 2
rs61754648
HDAC4
2 239090026 missense variant C/T snv 1.4E-03 1.8E-03 1
rs7180942
NTRK3
15 88131345 intron variant T/C snv 0.56 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs6189
NR3C1
0.827 0.240 5 143400774 missense variant C/A;T snv 4.0E-06; 1.8E-02 6