ClinVar Miner

Submissions for variant NM_052989.3(IFT122):c.42-6G>T

dbSNP: rs757753414
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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 RCV002122298 SCV002398202 likely benign Cranioectodermal dysplasia 1 2021-10-04 criteria provided, single submitter clinical testing

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