ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.78C>A (p.Gly26=)

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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 RCV002711434 SCV002999807 likely benign Hereditary spastic paraplegia 7 2022-11-15 criteria provided, single submitter clinical testing

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