ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.1892-17A>G

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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 RCV003601673 SCV004489759 likely benign Hereditary spastic paraplegia 11 2023-03-09 criteria provided, single submitter clinical testing

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