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: rs28934908
rs28934908
0.715 0.250 X 154031409 missense variant G/A,T snp 5.5E-06
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.710 1.000 7 2000 2007
dbSNP: rs62915962
rs62915962
0.821 0.179 X 154030632 missense variant G/A snp 5.1E-05 9.7E-05
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 2 2001 2002
dbSNP: rs61748392
rs61748392
0.801 0.214 X 154031418 missense variant T/C snp
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1 2001 2001
dbSNP: rs61748420
rs61748420
0.784 0.214 X 154031329 missense variant G/A,T snp
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1 2001 2001
dbSNP: rs61749715
rs61749715
0.744 0.179 X 154031154 missense variant G/A,C snp
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1 2003 2003
dbSNP: rs61750255
rs61750255
0.821 0.179 X 154030978 missense variant T/C snp
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1 2001 2001
dbSNP: rs61751449
rs61751449
0.756 0.179 X 154030864 missense variant G/A,C snp
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1 2006 2006
dbSNP: rs61753980
rs61753980
0.821 0.179 X 154030470 missense variant C/A,T snp 1.1E-05
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1 2001 2001