Source: GWASCAT

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 5
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs988712
BDNF-AS
0.925 0.160 11 27541835 intron variant G/A;T snv 1
rs10835211
BDNF ; BDNF-AS
1.000 0.080 11 27679818 intron variant G/A snv 0.19 1