ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.46C>T (p.Leu16=)

dbSNP: rs1443431827
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000596187 SCV000706619 uncertain significance not provided 2017-03-08 criteria provided, single submitter clinical testing
Invitae RCV003767383 SCV004604236 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2023-09-13 criteria provided, single submitter clinical testing

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