ClinVar Miner

Submissions for variant NM_213655.5(WNK1):c.2511G>A (p.Pro837=)

dbSNP: rs1024009612
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001503765 SCV001708623 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2023-06-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001503765 SCV002807818 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2021-12-24 criteria provided, single submitter clinical testing

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