ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.1015-3_1015-2del

dbSNP: rs1559245013
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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 RCV001486349 SCV001690805 likely benign Multiple sulfatase deficiency 2024-02-12 criteria provided, single submitter clinical testing

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