ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.-308G>T

dbSNP: rs886049861
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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 RCV000271081 SCV000381190 uncertain significance Hereditary sensory and autonomic neuropathy type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000326554 SCV000381191 uncertain significance Pseudohypoaldosteronism type 2A 2016-06-14 criteria provided, single submitter clinical testing

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