ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.114G>A (p.Gly38=)

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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 RCV003059248 SCV003334962 likely benign Multiple sulfatase deficiency 2022-04-01 criteria provided, single submitter clinical testing

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