ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.894G>A (p.Gly298=)

dbSNP: rs1300966652
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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 RCV002155232 SCV002417822 likely benign Cranioectodermal dysplasia 1 2022-11-14 criteria provided, single submitter clinical testing

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