ClinVar Miner

Submissions for variant NM_020800.3(IFT80):c.1665-7del

dbSNP: rs769406658
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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 RCV001510673 SCV001717769 benign Jeune thoracic dystrophy 2023-09-23 criteria provided, single submitter clinical testing

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