Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 40
rs1555565492
RAI1
0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs28935468
MECP2
0.732 0.240 X 154030912 missense variant G/A snv 14
rs587783405
CDKL5
0.851 0.160 X 18588021 stop gained C/T snv 9