ClinVar Miner

List of variants in gene GABRG2 reported as uncertain significance for Severe myoclonic epilepsy in infancy

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.-4del	rs771282908
NM_198904.4(GABRG2):c.-4dup	rs771282908

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