List of variants in gene MYPN reported as likely pathogenic for hereditary skeletal muscle disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.1317+1G>A	rs766502564
NM_032578.4(MYPN):c.1722dup (p.Lys575fs)
NM_032578.4(MYPN):c.1903C>T (p.Gln635Ter)
NM_032578.4(MYPN):c.295C>T (p.Arg99Ter)	rs756823228
NM_032578.4(MYPN):c.55_56del (p.Ser19fs)

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