ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.444+15G>A

dbSNP: rs2125133416
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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 RCV002192616 SCV002351121 likely benign Multiple sulfatase deficiency 2021-04-28 criteria provided, single submitter clinical testing

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