ClinVar Miner

Submissions for variant NM_000543.5(SMPD1):c.1098G>C (p.Gly366=)

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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 RCV003801820 SCV004597099 likely benign Niemann-Pick disease, type B; Niemann-Pick disease, type A 2024-02-04 criteria provided, single submitter clinical testing

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