ClinVar Miner

Submissions for variant NM_000202.8(IDS):c.534C>T (p.Leu178=)

dbSNP: rs2124047211
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001464644 SCV001668618 likely benign Mucopolysaccharidosis, MPS-II 2019-09-30 criteria provided, single submitter clinical testing

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