rs80338960, SCN4A

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Normokalemic Periodic Paralysis, Potassium-Sensitive
CUI: C1868433
Disease: Normokalemic Periodic Paralysis, Potassium-Sensitive
0.700 CausalMutation CLINVAR Hyperkalemic periodic paralysis and paramyotonia congenita--a novel sodium channel mutation. 11757950 2001
Hyperkalemic periodic paralysis
CUI: C0238357
Disease: Hyperkalemic periodic paralysis
0.700 CausalMutation CLINVAR Hyperkalemic periodic paralysis and paramyotonia congenita--a novel sodium channel mutation. 11757950 2001