ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.366C>G (p.Thr122=)

dbSNP: rs2102789624
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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 RCV001434743 SCV001637555 likely benign Hereditary antithrombin deficiency 2019-12-03 criteria provided, single submitter clinical testing

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