ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.1147+10A>T

gnomAD frequency: 0.00001  dbSNP: rs750848733
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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 RCV002539440 SCV001039995 likely benign Cranioectodermal dysplasia 1 2022-11-11 criteria provided, single submitter clinical testing

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