ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.5742C>A (p.Ile1914=)

dbSNP: rs1391710406
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002116341 SCV002442446 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2022-03-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002116341 SCV002798602 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2021-11-03 criteria provided, single submitter clinical testing

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