ClinVar Miner

Submissions for variant NM_018979.4(WNK1):c.108G>C (p.Gly36=) (rs375485682)

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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 RCV000348160 SCV000381220 uncertain significance Pseudohypoaldosteronism, type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000391432 SCV000381221 uncertain significance Hereditary sensory and autonomic neuropathy type II 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000647860 SCV000769663 likely benign Hereditary sensory and autonomic neuropathy type IIA; Pseudohypoaldosteronism type 2C 2017-09-11 criteria provided, single submitter clinical testing

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