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
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs6693503 1.000 0.040 1 19660801 upstream gene variant A/G snv 0.55 1
rs4912138
HTR6
1.000 0.040 1 19666992 intron variant A/G;T snv 1