ClinVar Miner

Submissions for variant NM_001371279.1(REEP1):c.784-20_784-19delinsTG

dbSNP: rs2103944805
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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 RCV002099033 SCV002431694 likely benign Hereditary spastic paraplegia 31 2022-10-28 criteria provided, single submitter clinical testing

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