Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998675361
POGZ
1.000 0.040 1 151430806 missense variant G/A;C snv 9.0E-06 1
rs966805126
NLGN1
1.000 0.040 3 173604861 missense variant C/T snv 1
rs963968092
EDNRA
0.882 0.120 4 147485844 missense variant A/C;G snv 8.0E-06 3
rs9616915
SHANK3
1.000 0.040 22 50679152 missense variant T/C snv 0.43 0.46 2
rs9468304
ELOVL2-AS1 ; ELOVL2
1.000 0.040 6 11041932 intron variant G/A snv 0.19 2
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs888864913
POGZ
1.000 0.040 1 151424097 missense variant C/T snv 1.2E-05 2.8E-05 1
rs886039770
TOP2B
1.000 0.040 3 25645353 missense variant G/A snv 1
rs886037776
EHMT1
0.925 0.280 9 137817477 stop gained G/A snv 2
rs878853161
SLC2A1
0.851 0.240 1 42929977 frameshift variant AT/- del 7
rs878853147
NLGN3
0.925 0.200 X 71169399 missense variant C/T snv 3
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 7
rs866632178
POGZ
1.000 0.040 1 151441000 missense variant C/T snv 1.6E-05 1.4E-05 1
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs8068149
NOS2
1.000 0.040 17 27761829 intron variant G/A snv 0.48 1
rs797045050
KIF1A
0.807 0.120 2 240797715 missense variant C/T snv 6
rs79667838
GRPR
0.882 0.120 X 16150432 missense variant C/T snv 3.0E-04 4.8E-04 3
rs796053483
TSC2
1.000 0.040 16 2060775 missense variant C/G snv 7.0E-06 1
rs796052733
MEF2C
1.000 0.040 5 88731773 stop gained G/A snv 1
rs782521991
RPL10 ; DNASE1L1 ; SNORA70
0.925 0.040 X 154400848 missense variant C/G snv 3.5E-05 2.8E-05 2
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs779545541
GPHN
0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 5
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs778792467
POGZ
1.000 0.040 1 151405692 missense variant G/C snv 4.4E-05 7.0E-06 1