ClinVar Miner

Submissions for variant NM_015161.3(ARL6IP1):c.170+15A>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 RCV003828479 SCV004623648 likely benign Hereditary spastic paraplegia 61 2023-12-27 criteria provided, single submitter clinical testing

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