ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.*1411G>A (rs148318176)

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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 RCV000264333 SCV000468991 uncertain significance Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000324544 SCV000468992 uncertain significance Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000379125 SCV000468993 uncertain significance Polydactyly 2016-06-14 criteria provided, single submitter clinical testing

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