List of variants in gene combination LOC130067861, SCO2 reported as uncertain significance for congenital structural 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005138.3(SCO2):c.-83A>G	rs886057632	0.00006
NM_005138.3(SCO2):c.-51C>T	rs886057631	0.00001

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