ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.5510-13G>A

gnomAD frequency: 0.00031  dbSNP: rs372263017
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002100747 SCV002383400 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2023-09-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002100747 SCV002811437 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2021-10-25 criteria provided, single submitter clinical testing

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