ClinVar Miner

Submissions for variant NM_000046.5(ARSB):c.267G>A (p.Pro89=)

dbSNP: rs573453966
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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 RCV002153809 SCV002462962 likely benign Mucopolysaccharidosis type 6 2023-10-15 criteria provided, single submitter clinical testing

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