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
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2070951
NR3C2
0.776 0.320 4 148436862 splice region variant G/A;C snv 4.2E-06; 0.53 9
rs2740210
OXT ; LOC101929098
0.827 0.120 20 3072609 downstream gene variant C/A snv 0.28 7
rs237885
CAV3 ; OXTR
0.925 0.080 3 8753857 intron variant T/G snv 0.53 3