ClinVar Miner

Submissions for variant NM_000295.5(SERPINA1):c.631T>C (p.Tyr211His)

dbSNP: rs864622052
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
HerediLab, Inc. RCV000205451 SCV000259200 likely benign Alpha-1-antitrypsin deficiency 2015-08-17 criteria provided, single submitter research

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