ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.710-29G>A

gnomAD frequency: 0.01046  dbSNP: rs72873478
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001000294 SCV001156954 benign Polycystic kidney disease 2 2019-03-01 criteria provided, single submitter clinical testing
GeneDx RCV001555304 SCV001776696 likely benign not provided 2020-04-28 criteria provided, single submitter clinical testing

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