List of variants in gene CHRND reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000751.3(CHRND):c.1105C>T (p.Pro369Ser)	rs2229194	0.00293
NM_000751.3(CHRND):c.862C>G (p.Gln288Glu)	rs41265127	0.00233
NM_000751.3(CHRND):c.1530C>T (p.Asn510=)	rs114463490	0.00155
NM_000751.3(CHRND):c.*676G>A	rs183259359	0.00042

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