ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.5510-7_5510-4del

dbSNP: rs1592219606
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001436784 SCV001639628 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2022-07-19 criteria provided, single submitter clinical testing

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