ClinVar Miner

Submissions for variant NM_005154.5(USP8):c.297C>A (p.Val99=)

dbSNP: rs183341645
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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 RCV000875327 SCV001017637 likely benign Hereditary spastic paraplegia 2019-12-31 criteria provided, single submitter clinical testing

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