ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.988-12G>C

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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 RCV002770993 SCV003033251 likely benign Hereditary spastic paraplegia 7 2023-11-27 criteria provided, single submitter clinical testing

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