ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.3292-17T>C

gnomAD frequency: 0.00001  dbSNP: rs1284535585
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002132607 SCV002435633 likely benign Hereditary spastic paraplegia 11 2024-08-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706382 SCV005214612 likely benign not provided criteria provided, single submitter not provided

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