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
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs496250
FXR1
0.851 0.080 3 180909515 intron variant G/A snv 0.24 5
rs12630592
GSK3B
0.851 0.080 3 120049399 intron variant G/A;T snv 5
rs2227283
GRIK2
0.882 0.080 6 102055442 missense variant G/A;C;T snv 0.40; 4.0E-06 3
rs6922753
GRIK2
1.000 0.040 6 101799798 splice region variant T/C snv 0.25 0.26 1