ClinVar Miner

Submissions for variant NM_000046.5(ARSB):c.789G>A (p.Arg263=)

dbSNP: rs2112483929
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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 RCV001448946 SCV001652050 likely benign Mucopolysaccharidosis type 6 2022-03-25 criteria provided, single submitter clinical testing

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