ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.277C>T (p.Arg93Cys)

dbSNP: rs764731214
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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 RCV001848188 SCV002105694 uncertain significance Hereditary spastic paraplegia 2021-06-16 criteria provided, single submitter clinical testing

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