Source: ALL
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 0.15 272
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs211037
GABRG2
0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs2292096
CAMSAP2
0.925 0.040 1 200857641 3 prime UTR variant A/G snv 0.14 2
rs210987
GABRG2
0.925 0.080 5 162108749 intron variant C/T snv 0.54 2
rs211014
GABRG2
0.925 0.080 5 162149412 3 prime UTR variant C/A snv 0.30 2
rs401750
GABRG2
0.925 0.040 5 162155655 3 prime UTR variant C/T snv 0.43 2
rs2422106
GABRG2
1.000 5 162134797 intron variant G/A;T snv 1