ClinVar Miner

Submissions for variant NM_173543.3(DZIP1L):c.1933A>G (p.Lys645Glu)

gnomAD frequency: 0.65135  dbSNP: rs442800
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001653293 SCV001871552 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001659248 SCV001875881 benign Polycystic kidney disease 5 2021-07-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001653293 SCV002406639 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001653293 SCV005300188 benign not provided criteria provided, single submitter not provided

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