ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.2529G>A (p.Gln843=) (rs9804992)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000405097 SCV000381845 benign Hereditary sensory and autonomic neuropathy type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000281228 SCV000381846 benign Pseudohypoaldosteronism, type 2 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000254165 SCV000313290 benign not specified criteria provided, single submitter clinical testing

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