ClinVar Miner

Submissions for variant NM_000202.8(IDS):c.708+19G>T

gnomAD frequency: 0.00003  dbSNP: rs782662196
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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 RCV003867962 SCV004664256 likely benign Mucopolysaccharidosis, MPS-II 2024-01-15 criteria provided, single submitter clinical testing

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