ClinVar Miner

Submissions for variant NM_182758.4(WDR72):c.955-43C>A

gnomAD frequency: 0.95246  dbSNP: rs690235
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001657122 SCV001867205 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243373 SCV002514946 benign Amelogenesis imperfecta hypomaturation type 2A3 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001657122 SCV005289324 benign not provided criteria provided, single submitter not provided

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