List of variants in gene combination GAA, LOC130061897 reported as uncertain significance for cardiomyopathy

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_000152.5(GAA):c.-312C>T	rs574326920	0.00161
NM_000152.5(GAA):c.-236C>T	rs886053541	0.00001

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