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rs104894299(C;C)

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common in clinvar

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

0

Good

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

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Is a genotype