ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.4968A>G (p.Glu1656=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV002511720 SCV002821678 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing WNK1: BP4, BP7
Invitae RCV002574750 SCV002936991 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C 2024-01-25 criteria provided, single submitter clinical testing

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