ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.2052A>G (p.Ala684=) (rs72648690)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000403369 SCV000381825 likely benign Hereditary sensory and autonomic neuropathy type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000312234 SCV000381826 likely benign Pseudohypoaldosteronism type 2A 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000550151 SCV000649401 benign not provided 2019-02-22 criteria provided, single submitter clinical testing

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