ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.*1780C>T (rs886062319)

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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 RCV000375671 SCV000468973 uncertain significance Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000281116 SCV000468974 uncertain significance Polydactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000322199 SCV000468975 uncertain significance Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing

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