Disease: MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs483353046
rs483353046
Entrez Id: 1134
Gene Symbol: CHRNA1
CHRNA1
CUI: C4084823
Disease:
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL 		A 0.700 CausalMutation CLINVAR
dbSNP: rs483353046
rs483353046
Entrez Id: 1134
Gene Symbol: CHRNA1
CHRNA1
CUI: C4084823
Disease:
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL 		T 0.700 CausalMutation CLINVAR