ClinVar Miner

Submissions for variant NM_001271620.2(ZNF423):c.1706A>G (p.Asn569Ser) (rs34214571)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000249143 SCV000312333 benign not specified criteria provided, single submitter clinical testing
Invitae RCV000544539 SCV000652407 benign Nephronophthisis 14 2019-12-31 criteria provided, single submitter clinical testing

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