ClinVar Miner

Submissions for variant NM_000235.4(LIPA):c.895-13A>G

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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 RCV003823939 SCV004624792 likely benign Wolman disease 2024-01-09 criteria provided, single submitter clinical testing

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