Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878853152
CUL4B
1.000 0.200 X 120547154 frameshift variant TG/- delins 1
rs878853151
KDM5C
1.000 0.200 X 53211601 frameshift variant -/A delins 1
rs878853149
TCF4
0.925 0.240 18 55350388 stop gained G/A snv 2
rs878853148
PHF8
1.000 0.200 X 54002150 splice region variant C/G snv 1
rs878853147
NLGN3
0.925 0.200 X 71169399 missense variant C/T snv 3
rs878853146
IL1RAPL1
1.000 0.200 X 29917576 frameshift variant TTGGGAAAGT/- delins 1
rs878853145
PQBP1 ; SLC35A2
1.000 0.200 X 48903017 missense variant C/T snv 1
rs878853144
IQSEC2
1.000 0.200 X 53239213 stop gained G/A snv 1
rs878853143
GRIN1
0.925 0.200 9 137162209 missense variant C/G;T snv 2
rs878853142
RAI1
1.000 0.200 17 17795278 frameshift variant GGCAT/- delins 1
rs878853141
KDM5C ; MIR6894
1.000 0.200 X 53199068 missense variant C/G snv 1
rs869312674
SYNGAP1
0.925 0.200 6 33446569 splice region variant G/A;C snv 4.0E-06 2
rs869025287
MED13L
0.925 0.200 12 115969040 frameshift variant GCCAATAT/- delins 2
rs864309503
MORC2
0.882 0.200 22 30941503 missense variant G/A snv 5
rs796053290
SLC9A6
0.925 0.280 X 135998095 splice region variant TTTTA/- delins 2
rs794729221
SLC2A1
0.925 0.240 1 42929736 stop gained G/A snv 2
rs765556214
GRIA4
1.000 0.200 11 105933765 missense variant G/A;C snv 1.6E-05 4.9E-05 1
rs762578331
UPF3B
0.925 0.200 X 119837939 missense variant G/A;T snv 8.2E-05; 5.5E-06 3
rs752306
DRD4
0.925 0.200 11 637622 intron variant C/T snv 6.4E-02 4.8E-02 3
rs752298579
TANGO2
0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs749457448
DLG3 ; DLG3-AS1
1.000 0.200 X 70452622 start lost A/G snv 2
rs745986648
SGO1-AS1 ; SGO1
1.000 0.200 3 20174431 missense variant C/T snv 1.2E-05 7.0E-06 2
rs724159950
DYRK1A ; LOC105372797
1.000 0.200 21 37486571 frameshift variant TGAG/GAA delins 6
rs724159949
LOC105372797 ; DYRK1A
0.827 0.240 21 37486563 stop gained C/T snv 15
rs723744
TTR
0.925 0.200 18 31592513 intron variant G/T snv 0.38 3