ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.-47C>T (rs886062341)

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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 RCV000400341 SCV000469314 uncertain significance Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000313234 SCV000469315 uncertain significance Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000345019 SCV000469316 uncertain significance Polydactyly 2016-06-14 criteria provided, single submitter clinical testing

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