ClinVar Miner

Submissions for variant NM_005619.5(RTN2):c.68A>G (p.Asp23Gly)

dbSNP: rs2122229330
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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 RCV001847512 SCV002104946 uncertain significance Hereditary spastic paraplegia 2021-03-15 criteria provided, single submitter clinical testing

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