ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.3531C>T (p.Leu1177=)

dbSNP: rs2137634680
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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 RCV001393745 SCV001595419 likely benign Spastic paraplegia 2021-07-14 criteria provided, single submitter clinical testing

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