ClinVar Miner

Submissions for variant NM_000235.4(LIPA):c.675+11C>T

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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 RCV003494854 SCV004301256 likely benign Wolman disease 2023-01-03 criteria provided, single submitter clinical testing

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