ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.201C>T (p.Gly67=)

gnomAD frequency: 0.00002  dbSNP: rs773751914
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 RCV001432689 SCV001635465 likely benign Hereditary antithrombin deficiency 2018-08-22 criteria provided, single submitter clinical testing

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