ClinVar Miner

Submissions for variant NM_001001331.4(ATP2B2):c.405G>A (p.Ala135=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002720256 SCV002991567 likely benign not provided 2022-08-05 criteria provided, single submitter clinical testing

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