ClinVar Miner

Submissions for variant NM_000295.5(SERPINA1):c.828C>T (p.Phe276=)

dbSNP: rs1566753494
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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 RCV002075818 SCV002388548 likely benign Alpha-1-antitrypsin deficiency 2021-08-28 criteria provided, single submitter clinical testing

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