ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.1207G>A (p.Val403Ile) (rs201070431)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193696 SCV000247479 likely benign not specified 2015-04-15 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000365900 SCV000469239 uncertain significance Polydactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000268836 SCV000469240 uncertain significance Greig cephalopolysyndactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000326204 SCV000469241 uncertain significance Pallister-Hall syndrome 2016-06-14 criteria provided, single submitter clinical testing

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