ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.6755-17C>T

gnomAD frequency: 0.00001  dbSNP: rs1595817791
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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 RCV002121240 SCV002449141 likely benign Hereditary spastic paraplegia 11 2023-12-10 criteria provided, single submitter clinical testing

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