ClinVar Miner

Submissions for variant NM_001191061.2(SLC25A22):c.210T>G (p.Ala70=)

dbSNP: rs1864648097
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002144932 SCV002414502 likely benign Early infantile epileptic encephalopathy with suppression bursts 2024-04-15 criteria provided, single submitter clinical testing
AiLife Diagnostics, AiLife Diagnostics RCV002224146 SCV002503266 uncertain significance not provided 2020-04-29 criteria provided, single submitter clinical testing

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