ClinVar Miner

Submissions for variant NM_000224.3(KRT18):c.599A>G (p.Glu200Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Intergen, Intergen Genetics and Rare Diseases Diagnosis Center RCV003985250 SCV004801396 uncertain significance Cirrhosis, familial 2024-03-19 criteria provided, single submitter clinical testing

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