ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.11317T>C (p.Leu3773=)

dbSNP: rs1194302679
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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 RCV002179296 SCV002482089 likely benign Spastic paraplegia 2021-07-06 criteria provided, single submitter clinical testing

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