ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.2689C>T (p.Pro897Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004797256 SCV005415717 uncertain significance Greig cephalopolysyndactyly syndrome; Pallister-Hall syndrome; Polysyndactyly 4; Polydactyly, postaxial, type A1 criteria provided, single submitter clinical testing PM2_Supporting+PP3_Moderate+PP1+PP4

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