ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.4590C>T (p.Asn1530=) (rs886062335)

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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 RCV000384316 SCV000469099 uncertain significance Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000289868 SCV000469100 uncertain significance Polydactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000326195 SCV000469101 uncertain significance Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing

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