ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.1371+251C>T

gnomAD frequency: 0.01682  dbSNP: rs11882991
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001678769 SCV001904466 benign not provided 2018-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001678769 SCV005307973 benign not provided criteria provided, single submitter not provided

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