Source: BEFREE

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 0.15 264
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs1415125856
BDNF ; BDNF-AS
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05 7
rs2030324
BDNF
0.827 0.120 11 27705368 intron variant A/G snv 0.49 6
rs56164415
BDNF
0.851 0.120 11 27700188 5 prime UTR variant G/A snv 5.9E-02 6
rs370102323
BDNF ; BDNF-AS
0.925 0.080 11 27658085 synonymous variant C/A;T snv 4.0E-06; 4.4E-05 2
rs1048218
BDNF-AS ; BDNF
1.000 0.080 11 27658340 missense variant C/A snv 1
rs756240390
BDNF ; BDNF-AS
1.000 0.080 11 27658370 synonymous variant G/A snv 4.0E-05 1.4E-05 1