ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.417G>A (p.Lys139=)

dbSNP: rs2102786232
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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 RCV002215138 SCV002361990 likely benign Hereditary antithrombin deficiency 2021-06-05 criteria provided, single submitter clinical testing

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