List of variants in gene STAC3 reported as likely pathogenic for congenital myopathy

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_145064.3(STAC3):c.851G>C (p.Trp284Ser)	rs140291094	0.00039
NM_145064.3(STAC3):c.432+1G>A	rs780801708	0.00002
NM_145064.3(STAC3):c.670+2T>A
NM_145064.3(STAC3):c.88_91del (p.Leu30fs)

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