ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.795C>T (p.Phe265=)

dbSNP: rs2077133706
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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 RCV002106797 SCV002324786 likely benign Cranioectodermal dysplasia 1 2024-01-31 criteria provided, single submitter clinical testing

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