ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.2336C>T (p.Ala779Val) (rs141428612)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000269146 SCV000381837 likely benign Hereditary sensory and autonomic neuropathy type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000326506 SCV000381838 likely benign Pseudohypoaldosteronism, type 2 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000553966 SCV000649407 benign not provided 2019-01-25 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000732756 SCV000860742 likely benign not specified 2018-04-05 criteria provided, single submitter clinical testing

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