ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.99C>T (p.His33=)

gnomAD frequency: 0.00003  dbSNP: rs147676453
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002109848 SCV002398178 likely benign Hereditary antithrombin deficiency 2023-08-18 criteria provided, single submitter clinical testing

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