ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.6069C>T (p.Ile2023=)

dbSNP: rs753141662
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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 RCV001492786 SCV001697406 likely benign Hereditary spastic paraplegia 11 2019-05-03 criteria provided, single submitter clinical testing

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