ClinVar Miner

Submissions for variant NM_000342.4(SLC4A1):c.702C>T (p.Ala234=)

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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 RCV002971688 SCV003286651 benign not provided 2024-05-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002971688 SCV005074534 likely benign not provided 2024-06-01 criteria provided, single submitter clinical testing SLC4A1: BP4, BP7

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