ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.1056C>T (p.Asn352=)

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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 RCV003606008 SCV004388203 likely benign Multiple sulfatase deficiency 2024-01-24 criteria provided, single submitter clinical testing

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