Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16917204
rs16917204
BDNF-AS
5 0.827 0.160 11 27646808 intron variant G/C snv 0.17 0.010 1.000 1 2015 2015
dbSNP: rs16917234
rs16917234
BDNF ; BDNF-AS
2 0.925 0.080 11 27676827 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs2030324
rs2030324
BDNF
6 0.827 0.120 11 27705368 intron variant A/G snv 0.49 0.010 1.000 1 2015 2015
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2004 2004