ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.5481A>G (p.Thr1827=) (rs61736908)

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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 RCV000277879 SCV000382000 likely benign Hereditary sensory and autonomic neuropathy type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000330500 SCV000382001 likely benign Pseudohypoaldosteronism, type 2 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000555944 SCV000649450 benign not provided 2019-01-29 criteria provided, single submitter clinical testing

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