ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.1644G>T (p.Leu548=)

dbSNP: rs1211494967
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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 RCV002217785 SCV002374546 likely benign Cranioectodermal dysplasia 1 2022-07-05 criteria provided, single submitter clinical testing

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