ClinVar Miner

Submissions for variant NM_000921.5(PDE3A):c.2769+30C>T

gnomAD frequency: 0.89678  dbSNP: rs9284155
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001678137 SCV001892584 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788746 SCV002029497 benign Brachydactyly-arterial hypertension syndrome 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001678137 SCV005236180 benign not provided criteria provided, single submitter not provided

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