Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338792
rs80338792
SCN4A
CUI: C2931826
Disease: Potassium aggravated myotonia
Potassium aggravated myotonia 		A 0.820 CausalMutation CLINVAR

dbSNP: rs80338792
rs80338792
SCN4A
CUI: C2931826
Disease: Potassium aggravated myotonia
Potassium aggravated myotonia 		T 0.820 CausalMutation CLINVAR

dbSNP: rs80338792
rs80338792
SCN4A
CUI: C2931826
Disease: Potassium aggravated myotonia
Potassium aggravated myotonia 		G 0.820 CausalMutation CLINVAR