ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.4636-11_4636-10del

dbSNP: rs765481566
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000367443 SCV000391282 uncertain significance Spastic Paraplegia, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002520960 SCV003031183 likely benign Hereditary spastic paraplegia 11 2023-12-01 criteria provided, single submitter clinical testing

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