Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs179363900
rs179363900
MECP2
6 0.807 0.080 X 154031374 missense variant G/C snv 5.5E-06 1.9E-05 0.700 0
dbSNP: rs28934904
rs28934904
MECP2
9 0.776 0.200 X 154031431 missense variant G/A;C;T snv 0.700 0