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
rs1565228
BDNF-AS
11 27564889 intron variant G/A;C snv 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs16917237
BDNF ; BDNF-AS
11 27680836 intron variant G/T snv 0.16 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs10767658
BDNF-AS
11 27650705 intron variant C/G;T snv 2
rs1519480
BDNF-AS
0.925 0.040 11 27654165 intron variant C/T snv 0.54 2
rs2049045
BDNF-AS ; BDNF
1.000 0.080 11 27672694 intron variant G/A;C snv 0.13 2
rs10767654
BDNF-AS ; LINC00678
11 27618676 intron variant T/G snv 0.73 2
rs4923460
BDNF-AS ; LINC00678
11 27635242 intron variant G/T snv 0.20 2
rs11030102
BDNF ; BDNF-AS
11 27660049 non coding transcript exon variant C/G snv 0.19 2
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 2
rs2029362
BDNF-AS
11 27584586 intron variant C/T snv 0.40 1
rs988712
BDNF-AS
0.925 0.160 11 27541835 intron variant G/A;T snv 1
rs17309874
BDNF-AS
11 27645689 intron variant G/A snv 0.19 1
rs10501087
BDNF-AS
11 27648561 intron variant T/C snv 0.17 1
rs35051342
BDNF-AS
11 27612826 intron variant G/C snv 0.16 1
rs6416056
BDNF-AS ; LINC00678
11 27625198 intron variant G/A snv 0.71 1
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 1
rs61888762
BDNF ; BDNF-AS
11 27688083 intron variant C/G snv 0.27 1
rs4517468
BDNF ; BDNF-AS
11 27666739 intron variant A/T snv 0.53 1
rs10835211
BDNF ; BDNF-AS
1.000 0.080 11 27679818 intron variant G/A snv 0.19 1
rs11030100
BDNF ; BDNF-AS
1.000 0.080 11 27656039 3 prime UTR variant G/T snv 0.17 1