Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs132630275
rs132630275
0.925 0.080 X 48684323 missense variant C/A;G snv
Thrombocytopenia, X-Linked, Intermittent
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs132630276
rs132630276
0.925 0.080 X 48689423 missense variant T/A snv
Thrombocytopenia, X-Linked, Intermittent
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 0