ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.4850+102C>T

gnomAD frequency: 0.01906  dbSNP: rs75650362
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 RCV001667808 SCV001887081 benign not provided 2019-04-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001667808 SCV005268369 benign not provided criteria provided, single submitter not provided

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