Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518921
MED12
1.000 X 71132465 missense variant G/A snv 7
rs542652468
ATP1A3
0.882 19 41986177 missense variant G/A;T snv 6
rs1559720382
SETD2
1.000 3 47101476 missense variant T/C snv 2
rs1567053134
CYP11A1
0.925 0.040 15 74345160 frameshift variant AG/- del 8
rs564185858
ADD3
0.882 0.040 10 110122249 missense variant G/A snv 1.2E-05 1.4E-05 4
rs121912708
ALDH7A1
1.000 0.040 5 126583997 stop gained G/A;C snv 6.0E-05; 4.0E-06 3
rs140845195
ALDH7A1
1.000 0.040 5 126545020 splice acceptor variant C/A;T snv 1.6E-05; 4.0E-06 3
rs1085308053
PTEN
0.882 0.080 10 87952230 missense variant C/T snv 5
rs1565977796
CDK8
0.882 0.120 13 26337623 stop gained C/A snv 7
rs267607093
SRD5A3
0.851 0.160 4 55359444 stop gained G/A snv 4.0E-06 14
rs1554823375
WDR37
0.851 0.160 10 1080454 missense variant C/T snv 8
rs1569234334
KIF4A
0.851 0.200 X 70329420 missense variant G/T snv 5
rs587777893
MTOR
0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs1556425596
COL6A1
0.752 0.240 21 45989967 intron variant C/T snv 37
rs758361736
KIF7
0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs397515415
HDAC8
0.807 0.240 X 72495216 stop gained G/A;T snv 10
rs797045412
BICD2
0.776 0.280 9 92718565 missense variant G/A;T snv 17
rs431905509
SLC25A1
0.807 0.280 22 19176222 missense variant G/A;C snv 2.0E-05 8
rs1554333853
CDK13
0.689 0.320 7 40046006 missense variant A/G snv 54
rs138659167
DHCR7
0.807 0.320 11 71435840 splice acceptor variant C/A;G snv 5.6E-05; 3.9E-03 20
rs1032242817
DHCR7
0.807 0.320 11 71441307 stop gained C/T snv 8.0E-06 7.0E-06 17
rs1554603293
CHD7
0.752 0.320 8 60849154 missense variant G/A snv 17
rs1555640521
LAMA1
0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs1569355102
DYRK1A
0.695 0.360 21 37472869 frameshift variant TAAC/- delins 51
rs1057519389
EBF3
0.695 0.400 10 129957324 missense variant C/A;G;T snv 46