List of variants in gene combination CCDC40, GAA reported as likely benign for Glycogen storage disease, type II

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_017950.4(CCDC40):c.*654A>C	rs2289538	0.02339
NM_017950.4(CCDC40):c.*265C>T	rs74000393	0.01774
NM_017950.4(CCDC40):c.3340G>A (p.Val1114Met)	rs61740509	0.00839
NM_000152.5(GAA):c.-75C>G	rs80020206

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