ClinVar Miner

Submissions for variant NM_198904.4(GABRG2):c.219G>A (p.Leu73=)

gnomAD frequency: 0.00004  dbSNP: rs753076158
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002315464 SCV000849383 likely benign Inborn genetic diseases 2017-04-07 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV001393017 SCV001594666 likely benign Epilepsy, childhood absence 2; Febrile seizures, familial, 8 2025-01-13 criteria provided, single submitter clinical testing
GeneDx RCV001709684 SCV001936911 benign not provided 2015-08-12 criteria provided, single submitter clinical testing

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