ClinVar Miner

Submissions for variant NM_000504.4(F10):c.270T>A (p.Cys90Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. Zeinali's Medical Genetics Lab, Kawsar Human Genetics Research Center RCV003445226 SCV003932670 likely pathogenic Hereditary factor X deficiency disease 2023-05-05 criteria provided, single submitter clinical testing

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