ClinVar Miner

Submissions for variant NM_001271803.2(REEP2):c.606G>A (p.Pro202=)

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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 RCV003583488 SCV004279320 likely benign Hereditary spastic paraplegia 72 2023-08-19 criteria provided, single submitter clinical testing

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