ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.1910A>G (p.Asn637Ser)

gnomAD frequency: 0.02773  dbSNP: rs34214571
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249143 SCV000312333 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000544539 SCV000652407 benign Nephronophthisis 14 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001618449 SCV001844902 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000544539 SCV002514223 benign Nephronophthisis 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001618449 SCV005289754 benign not provided criteria provided, single submitter not provided

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