ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.3284A>G (p.Asp1095Gly) (rs1554304659)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503551 SCV000594994 uncertain significance not specified 2016-05-17 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000764714 SCV000895848 uncertain significance Greig cephalopolysyndactyly syndrome; Hamartoma of hypothalamus; Pallister-Hall syndrome; Preaxial polydactyly 4; Postaxial polydactyly type A1 2018-10-31 criteria provided, single submitter clinical testing

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