ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.186A>G (p.Pro62=)

dbSNP: rs1452738609
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001732440 SCV001982507 likely benign not provided 2021-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005213561 SCV005853827 benign Greig cephalopolysyndactyly syndrome; Pallister-Hall syndrome 2024-10-24 criteria provided, single submitter clinical testing

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