ClinVar Miner

Submissions for variant NM_005220.3(DLX3):c.516+23C>T

gnomAD frequency: 0.18199  dbSNP: rs2303467
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001598959 SCV001827566 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658309 SCV001876775 benign Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism 2021-07-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658308 SCV001876776 benign Tricho-dento-osseous syndrome 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001598959 SCV005249876 benign not provided criteria provided, single submitter not provided

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