ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.2239-109G>A

gnomAD frequency: 0.00419  dbSNP: rs569349271
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 RCV001665579 SCV001880946 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001665579 SCV005268349 benign not provided criteria provided, single submitter not provided

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