ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.11715T>C (p.Leu3905=)

dbSNP: rs1593121777
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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 RCV001487195 SCV001691680 likely benign Spastic paraplegia 2022-02-11 criteria provided, single submitter clinical testing

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