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: rs61753980
rs61753980
MECP2
1 1.000 0.080 X 154030470 missense variant C/A;T snv 1.1E-05 0.700 1.000 10 2000 2007
dbSNP: rs61751444
rs61751444
MECP2
5 0.882 0.080 X 154030903 missense variant G/A snv 0.700 1.000 3 2007 2013