ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.1008+17T>G

dbSNP: rs2077967767
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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 RCV002128122 SCV002449996 likely benign Cranioectodermal dysplasia 1 2021-06-13 criteria provided, single submitter clinical testing

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