ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.1503C>T (p.Val501=)

dbSNP: rs2542396217
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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 RCV003591082 SCV004337187 likely benign Spastic paraplegia 2023-11-14 criteria provided, single submitter clinical testing

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