List of variants in gene ISCU reported as likely benign 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_213595.4(ISCU):c.419-162C>T	rs73404738	0.02683
NM_213595.4(ISCU):c.10G>C (p.Ala4Pro)	rs558084375	0.00362

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