ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.402C>G (p.Ala134=)

dbSNP: rs201360097
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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 RCV000872579 SCV001014411 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2024-01-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705838 SCV005211348 likely benign not provided criteria provided, single submitter not provided

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