ClinVar Miner

Submissions for variant NM_182758.4(WDR72):c.*1739G>A

gnomAD frequency: 0.37656  dbSNP: rs8041208
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000265596 SCV000393050 benign Amelogenesis Imperfecta, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715909 SCV005289316 benign not provided criteria provided, single submitter not provided

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