ClinVar Miner

Submissions for variant NM_001039.4(SCNN1G):c.776C>A (p.Thr259Asn) (rs72646501)

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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 RCV000341227 SCV000395728 uncertain significance Pseudohypoaldosteronism type 1 autosomal recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000399950 SCV000395729 uncertain significance Liddle syndrome 1 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000713394 SCV000843995 uncertain significance not provided 2017-09-30 criteria provided, single submitter clinical testing

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