Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2030324
BDNF
0.827 0.120 11 27705368 intron variant A/G snv 0.49 6
rs16917204
BDNF-AS
0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs16917234
BDNF ; BDNF-AS
0.925 0.080 11 27676827 intron variant T/A;C snv 2