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
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
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1325757098
TAT ; TAT-AS1
0.827 0.160 16 71576223 missense variant C/T snv 8.0E-06 7.0E-06 6
rs2478813
PLXNA2
0.882 0.080 1 208073865 intron variant A/G snv 0.85 4
rs12673132
NPSR1 ; NPSR1-AS1
0.925 7 34663912 intron variant G/A snv 4.2E-02 2
rs716461
PLXNA2
0.925 0.040 1 208084284 intron variant G/A snv 0.23 2