CST3, cystatin C, 1471

N. diseases: 370; N. variants: 10
Disease: Hereditary Cerebral Amyloid Angiopathy, Icelandic Type ×
Source: ALL
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: rs28939068
rs28939068 		0.790 0.200 20 23635330 missense variant A/T snv
CUI: C1527338
Disease: Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases 0.810 0.750 4 1989 2010