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
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs2072446
LOC100288866 ; MIR6165 ; NGFR
0.776 0.160 17 49510457 missense variant C/T snv 5.2E-02 4.1E-02 11
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs1415125856
BDNF ; BDNF-AS
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05 7
rs2049046
BDNF
0.827 0.200 11 27702228 intron variant T/A snv 0.48 6
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
rs727155 1.000 0.040 11 27728902 intron variant C/T snv 8.2E-02 1
rs7931247 1.000 0.040 11 27725444 intron variant T/C snv 0.48 1
rs2192371
HTR2C
1.000 0.040 X 114655361 intron variant G/A snv 1
rs55674402
HTR3D
1.000 0.040 3 184038954 synonymous variant C/T snv 0.37 0.33 1
rs144643855
LOC101929021 ; NEUROG3
1.000 0.040 10 69573087 intron variant TG/- del 0.23 1
rs11466155
NGFR ; LOC100288866 ; MIR6165
1.000 0.040 17 49510638 synonymous variant C/T snv 0.31 0.25 1
rs1778929
NTRK2
1.000 0.040 9 84707625 intron variant T/C snv 0.50 1
rs7816
NTRK2
1.000 0.040 9 84815606 3 prime UTR variant T/A snv 0.75 1
rs17406271
PIK3C2B
1.000 0.040 1 204427600 intron variant A/C snv 0.11 0.15 1
rs2271419
PIK3C2B
1.000 0.040 1 204429933 synonymous variant A/G snv 4.0E-06; 0.10 0.14 1
rs2271420
PIK3C2B
1.000 0.040 1 204429936 synonymous variant G/A;C snv 0.10; 4.0E-06 1
rs8178895
PLAT
1.000 0.040 8 42174861 3 prime UTR variant T/C snv 0.10 1
rs11204922
S100A10 ; LOC105371441
1.000 0.040 1 151989099 intron variant T/C snv 0.33 1
rs12837651
SNORA35 ; HTR2C
1.000 0.040 X 114629635 intron variant C/A;T snv 1