ClinVar Miner

Submissions for variant NC_000023.11:g.139529943A>G

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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 RCV002993667 SCV003290460 benign Hereditary factor IX deficiency disease; Thrombophilia, X-linked, due to factor 9 defect 2024-10-14 criteria provided, single submitter clinical testing

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