ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.5727G>A (p.Pro1909=)

dbSNP: rs763247767
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001503231 SCV001708083 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2019-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001503231 SCV002795523 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2021-11-08 criteria provided, single submitter clinical testing

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