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: rs121434622
rs121434622
1.000 0.080 X 147936534 missense variant T/A snv
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.860 1.000 11 1997 2015