ClinVar Miner

Submissions for variant NM_000921.5(PDE3A):c.1760+38A>C

gnomAD frequency: 0.61326  dbSNP: rs7304499
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001539297 SCV001757053 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788588 SCV002029496 benign Brachydactyly-arterial hypertension syndrome 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001539297 SCV005236167 benign not provided criteria provided, single submitter not provided

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