ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.396T>C (p.Ser132=)

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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 RCV005134244 SCV005756716 likely benign Multiple sulfatase deficiency 2024-06-07 criteria provided, single submitter clinical testing

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