Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs2070951
NR3C2
0.776 0.320 4 148436862 splice region variant G/A;C snv 4.2E-06; 0.53 9
rs2049046
BDNF
0.827 0.200 11 27702228 intron variant T/A snv 0.48 6
rs6190
NR3C1
0.827 0.120 5 143400772 missense variant C/G;T snv 4.0E-06; 1.8E-02 6
rs375382379
NR3C1
0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 5
rs550659379
NR3C1
0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs752834812
NR3C1
0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 5
rs772651364
NR3C1
0.882 0.160 5 143400050 missense variant C/T snv 4.0E-06 5
rs200889048 0.882 0.120 3 74928276 intergenic variant C/- del 3
rs373288445
DISC1 ; TSNAX-DISC1
0.925 0.080 1 231694534 missense variant C/T snv 5.6E-05 4.2E-05 3
rs773758385
DISC1 ; TSNAX-DISC1
0.925 0.080 1 231694162 missense variant C/T snv 1.0E-04 3.5E-05 3
rs12490016
LINC00880 ; LINC00881
0.882 0.120 3 157121142 intron variant G/C snv 4.6E-02 3
rs1630623
TMC1
0.882 0.120 9 72725323 intron variant A/G snv 0.29 3
rs4142324 1.000 0.040 15 50871860 intron variant C/T snv 0.29 1