ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.*1858C>T (rs886062318)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000369928 SCV000468970 uncertain significance Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000260965 SCV000468971 uncertain significance Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000316467 SCV000468972 uncertain significance Polydactyly 2016-06-14 criteria provided, single submitter clinical testing

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