List of variants in gene RAPSN reported as not provided for Congenital myasthenic syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005055.5(RAPSN):c.264C>A (p.Asn88Lys)	rs104894299	0.00149
NM_005055.5(RAPSN):c.-210A>G	rs786200905	0.00002
NM_005055.5(RAPSN):c.-199C>G	rs886037842

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