ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.*2071C>T

gnomAD frequency: 0.00004  dbSNP: rs539931592
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000363041 SCV000468964 likely benign Polydactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000404465 SCV000468965 likely benign Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000309568 SCV000468966 likely benign Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing

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