ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.72G>T (p.Leu24=)

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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 RCV003605294 SCV004452884 likely benign Multiple sulfatase deficiency 2023-04-03 criteria provided, single submitter clinical testing

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