ClinVar Miner

Submissions for variant NM_020800.3(IFT80):c.2224-19_2224-18dup

dbSNP: rs58665245
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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 RCV001509976 SCV001716898 benign Jeune thoracic dystrophy 2023-12-31 criteria provided, single submitter clinical testing

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