ClinVar Miner

Submissions for variant NM_000202.8(IDS):c.576C>G (p.Pro192=)

dbSNP: rs1286461259
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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 RCV003622340 SCV004553150 likely benign Mucopolysaccharidosis, MPS-II 2023-02-16 criteria provided, single submitter clinical testing

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