ClinVar Miner

Submissions for variant NM_032387.5(WNK4):c.3023-9G>A

gnomAD frequency: 0.00072  dbSNP: rs377609818
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002967390 SCV003286585 benign not provided 2025-01-31 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003961317 SCV004768976 likely benign WNK4-related disorder 2019-12-23 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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