ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.3492G>A (p.Val1164=)

dbSNP: rs778613425
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000994766 SCV001148509 uncertain significance not provided 2016-05-01 criteria provided, single submitter clinical testing
Invitae RCV002068719 SCV002345285 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2023-12-19 criteria provided, single submitter clinical testing

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