ClinVar Miner

Submissions for variant NM_000487.6(ARSA):c.685-5C>T

dbSNP: rs2146722799
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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 RCV002211695 SCV002351841 likely benign Metachromatic leukodystrophy 2022-05-30 criteria provided, single submitter clinical testing

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