ClinVar Miner

Submissions for variant NM_014946.4(SPAST):c.1174-16C>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 RCV003633993 SCV004524745 likely benign Hereditary spastic paraplegia 4 2023-10-05 criteria provided, single submitter clinical testing

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