rs104894299(A;A)

Congenital myasthenic syndrome

Is a	genotype
of	rs104894299
Gene	RAPSN
Chromosome	11
Position	47,448,079
mentioned	by

Magnitude

6

Repute

Bad

Geno	Mag	Summary
(A;A)	6	Congenital myasthenic syndrome
(A;C)	3	carrier of one Myasthenic syndrome allele
(C;C)	0	common in clinvar

see discussion at rs104894299