ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.*1904dup

gnomAD frequency: 0.00019  dbSNP: rs1555165765
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000358922 SCV000375232 uncertain significance Hereditary sensory and autonomic neuropathy type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000394051 SCV000375233 uncertain significance Pseudohypoaldosteronism type 2A 2016-06-14 criteria provided, single submitter clinical testing

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