ClinVar Miner

Submissions for variant NM_005619.5(RTN2):c.1484A>G (p.Tyr495Cys)

dbSNP: rs1037969877
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001847508 SCV002104937 uncertain significance Hereditary spastic paraplegia 2021-04-01 criteria provided, single submitter clinical testing

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