Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs375382379
NR3C1
0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 5
rs6189
NR3C1
0.827 0.240 5 143400774 missense variant C/A;T snv 4.0E-06; 1.8E-02 6
rs772651364
NR3C1
0.882 0.160 5 143400050 missense variant C/T snv 4.0E-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
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs752834812
NR3C1
0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 5
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs554073050
CCK
0.925 0.040 3 42263460 synonymous variant G/A snv 1.2E-05 7.0E-06 3
rs61754648
HDAC4
2 239090026 missense variant C/T snv 1.4E-03 1.8E-03 1
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs495225
GHSR
0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19