ClinVar Miner

Submissions for variant NM_173543.3(DZIP1L):c.1633A>G (p.Thr545Ala)

gnomAD frequency: 0.71390  dbSNP: rs446644
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001659263 SCV001875883 benign Polycystic kidney disease 5 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV001707913 SCV001934886 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001707913 SCV002339056 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001707913 SCV005302371 benign not provided criteria provided, single submitter not provided

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