ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.1937-9G>A

gnomAD frequency: 0.00026  dbSNP: rs371739639
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722616 SCV000716432 likely benign not provided 2020-09-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005091619 SCV005846603 likely benign Hereditary spastic paraplegia 7 2024-04-25 criteria provided, single submitter clinical testing

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