ClinVar Miner

Submissions for variant NM_014946.4(SPAST):c.87G>A (p.Leu29=)

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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 RCV003633892 SCV004384192 likely benign Hereditary spastic paraplegia 4 2024-07-31 criteria provided, single submitter clinical testing

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