ClinVar Miner

Submissions for variant NM_213655.5(WNK1):c.2145T>C (p.Arg715=)

dbSNP: rs1951533512
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001503519 SCV001708375 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2022-02-08 criteria provided, single submitter clinical testing

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