ClinVar Miner

Submissions for variant NM_000202.8(IDS):c.918T>C (p.Tyr306=)

gnomAD frequency: 0.00002  dbSNP: rs781920980
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 RCV001444470 SCV001647473 likely benign Mucopolysaccharidosis, MPS-II 2024-02-12 criteria provided, single submitter clinical testing

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