ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.3112-10C>T (rs72650715)

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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 RCV000353491 SCV000381936 likely benign Pseudohypoaldosteronism, type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000277516 SCV000381937 likely benign Hereditary sensory and autonomic neuropathy type II 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000534003 SCV000649414 likely benign Hereditary sensory and autonomic neuropathy type IIA; Pseudohypoaldosteronism type 2C 2017-12-13 criteria provided, single submitter clinical testing

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