ClinVar Miner

Submissions for variant NM_152415.3(VPS37A):c.699A>G (p.Glu233=)

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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 RCV002628811 SCV003515941 likely benign Hereditary spastic paraplegia 53 2022-06-03 criteria provided, single submitter clinical testing

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