Disease: Seizures
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs200661329
PIGQ
0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs1555462347
USP7
0.716 0.520 16 8901028 frameshift variant CT/- delins 34
rs1057524820
SCN8A
0.776 0.280 12 51765746 missense variant G/A;T snv 33
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs1057524157
DEAF1
0.776 0.200 11 686962 missense variant A/C;T snv 19
rs1554944271
DEAF1
0.851 0.240 11 686925 missense variant C/G snv 14
rs1131692231
CYFIP2
0.827 0.280 5 157294834 missense variant C/T snv 13
rs1555883505
EEF1A2
0.827 0.160 20 63490712 missense variant G/A snv 10
rs1064793575
SLC9A6
0.925 0.040 X 136016706 frameshift variant GT/- delins 6