List of variants in gene GFER 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005262.3(GFER):c.580C>T (p.Arg194Cys)	rs780851934	0.00003
NM_005262.3(GFER):c.259-25_259-24del	rs1597063303

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