Disease: Familial Periodic Paralysis ×
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: rs80338777
rs80338777 		0.827 0.200 1 201077915 missense variant C/A;T snv 1.2E-05
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2005 2005