Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11893842
OBSL1 ; INHA
0.925 0.160 2 219572251 intron variant A/G snv 0.45 2
rs778139192
KIF7 ; TICRR
0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 14
rs886041116
ADNP
0.776 0.240 20 50892526 stop gained G/A snv 13
rs121907917
PAX6
0.807 0.240 11 31794079 stop gained G/A snv 6
rs1057518951
ARID1B
0.827 0.160 6 156829296 stop gained C/T snv 5
rs754914260
DCC
0.925 0.120 18 52923832 stop gained C/A;T snv 4.0E-06 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 12
rs1190999960
ZNRD2-AS1 ; ZNRD2 ; FAM89B
0.807 0.240 11 65571690 missense variant G/A snv 9
rs1250394819
LOC101927100 ; TMED7-TICAM2 ; TMED7
0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06 9
rs568887534
DCTN6
0.807 0.240 8 30183156 missense variant A/G snv 4.0E-06 9
rs1064796460
TUBA1A
0.790 0.400 12 49185197 missense variant C/G;T snv 8
rs431905509
SLC25A1
0.807 0.280 22 19176222 missense variant G/A;C snv 2.0E-05 8
rs1555696625
NFIX
0.851 0.360 19 13025409 missense variant G/A snv 7
rs886039811
B9D1
0.807 0.320 17 19357875 missense variant A/G snv 4.0E-06 6
rs1569234334
KIF4A
0.851 0.200 X 70329420 missense variant G/T snv 5
rs797045005
TUBA1A
0.851 0.320 12 49185140 missense variant A/G snv 4
rs1057517858
TUBA1A
0.925 0.240 12 49185714 missense variant C/A;T snv 3
rs1057523157
SETD2
0.925 0.120 3 47088172 missense variant G/A snv 3
rs1563183469
AUTS2
0.925 0.120 7 70766245 missense variant A/C snv 3
rs1565627707
TUBA1A
0.925 0.240 12 49186657 missense variant C/A snv 3
rs199590018
SYP
0.925 0.120 X 49193294 missense variant G/A snv 1.4E-04 7.5E-05 3
rs387907252
VAX1
0.882 0.160 10 117134559 missense variant G/T snv 3
rs587780072
TP53
0.882 0.240 17 7674927 missense variant G/A;C snv 2.8E-05 3