ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.3098del (p.Lys1033fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005034969 SCV005661406 likely pathogenic Cranioectodermal dysplasia 1 2024-05-03 criteria provided, single submitter clinical testing

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