ClinVar Miner

Submissions for variant NM_014855.3(AP5Z1):c.465C>T (p.Pro155=)

dbSNP: rs758859483
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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 RCV001503655 SCV001708511 likely benign Hereditary spastic paraplegia 48 2020-06-14 criteria provided, single submitter clinical testing

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