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: rs386833427
rs386833427
4 177438848 missense variant A/G snv 7.0E-06
CUI: C0268225
Disease: Aspartylglucosaminuria
Aspartylglucosaminuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.800 0