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
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs7687423
NPY1R
0.925 0.080 4 163329645 intron variant A/G snv 0.53 3
rs6662926
TSNAX-DISC1
1.000 0.080 1 231567179 intron variant G/A;C snv 1
rs1630250
TSNAX-DISC1 ; TSNAX
1.000 0.080 1 231528457 5 prime UTR variant G/A;C snv 1