Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804833
MAP2K7
1.000 0.040 19 7905750 intron variant A/G;T snv 1
rs4977831
FOCAD
1.000 0.040 9 20713069 intron variant A/G;T snv 1
rs6502892
MIR22 ; MIR22HG
1.000 0.040 17 1714314 intron variant T/C;G snv 1
rs860554
PKP1
1.000 0.040 1 201293304 intron variant C/G;T snv 1
rs9302001
LOC101927284
1.000 0.040 13 94811138 intergenic variant C/A;T snv 1
rs1805067
SLC6A2
0.925 0.080 16 55698511 missense variant G/A snv 2.8E-05 2.1E-05 2
rs324891
LINC00461
1.000 0.040 5 88616114 intron variant C/T snv 4.2E-04 1
rs191260602
GLRB
1.000 0.040 4 157140489 intron variant A/G snv 7.7E-03 1
rs941184
CALCOCO1
1.000 0.040 12 53720374 intron variant C/T snv 3.6E-02 1
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs4145262 1.000 0.040 12 105659532 regulatory region variant C/A snv 4.8E-02 1
rs17260539 1.000 0.040 9 12182545 intergenic variant G/A snv 6.6E-02 1
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs11763020
C7orf50
1.000 0.040 7 1020652 intron variant C/T snv 0.12 1
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs8076112
TLCD2
1.000 0.040 17 1708905 intron variant A/C;G snv 0.15 1
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs4076452
LINC02210-CRHR1
1.000 0.040 17 45778528 intron variant G/C snv 0.16 2
rs1800857
CCKAR
0.851 0.120 4 26489489 splice region variant A/G snv 0.17 0.18 4