Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 9
rs10774547 0.925 0.120 12 120424913 intergenic variant T/C snv 0.39 3
rs59197085
CCDC136
0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02 3
rs1711745
INIP
0.925 0.120 9 112690629 intron variant C/A snv 0.13 3
rs5995177
RBFOX2
0.925 0.120 22 35913505 intron variant G/A;C snv 2
rs12121864 1.000 0.080 1 9145273 downstream gene variant C/A snv 5.2E-02 1
rs3787751
HLCS
1.000 0.080 21 36787862 intron variant T/A;C snv 1
rs10504229
LINC00588
1.000 0.080 8 57283936 intron variant A/G snv 0.16 1