ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.*3341dup

dbSNP: rs138425063
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000343252 SCV000468898 benign Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000403680 SCV000468899 benign Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000303316 SCV000468900 benign Polydactyly 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001537136 SCV001753975 benign not provided 2021-05-12 criteria provided, single submitter clinical testing

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