ClinVar Miner

List of variants in gene combination LOC129999670, PRKAG2 reported as uncertain significance for Lethal congenital glycogen storage disease of heart

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016203.3(PRKAG2):c.-575C>T	rs886062108
NM_016203.3(PRKAG2):c.-580C>T	rs886062109

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