Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs191260602
GLRB
1.000 0.040 4 157140489 intron variant A/G snv 7.7E-03 1
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs13356494 1.000 0.040 5 135991866 regulatory region variant C/G;T snv 1
rs324891
LINC00461
1.000 0.040 5 88616114 intron variant C/T snv 4.2E-04 1
rs37790 1.000 0.040 5 53346682 intergenic variant C/G;T snv 1
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs1418688 1.000 0.040 6 71169166 downstream gene variant A/G;T snv 1
rs9372078 1.000 0.040 6 150592825 intergenic variant T/A snv 0.73 1
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs11763020
C7orf50
1.000 0.040 7 1020652 intron variant C/T snv 0.12 1
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs17260539 1.000 0.040 9 12182545 intergenic variant G/A snv 6.6E-02 1
rs2039391
FOCAD
1.000 0.040 9 20714015 intron variant C/T snv 0.86 1
rs4977831
FOCAD
1.000 0.040 9 20713069 intron variant A/G;T snv 1
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
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36