ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.287-15C>G

gnomAD frequency: 0.00001  dbSNP: rs760006158
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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 RCV002132520 SCV002430923 likely benign Hereditary spastic paraplegia 7 2021-08-23 criteria provided, single submitter clinical testing

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