ClinVar Miner

Submissions for variant NM_015915.5(ATL1):c.283-20del

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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 RCV003503528 SCV004365049 likely benign Hereditary spastic paraplegia 3A 2023-12-15 criteria provided, single submitter clinical testing

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