ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.6805C>T (p.Leu2269=)

gnomAD frequency: 0.00001  dbSNP: rs781036043
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001424913 SCV001627521 likely benign Hereditary spastic paraplegia 11 2019-06-17 criteria provided, single submitter clinical testing

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