ClinVar Miner

Submissions for variant NM_001039.4(SCNN1G):c.*789_*790delinsCT

dbSNP: rs386789797
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000269807 SCV000395778 uncertain significance Liddle syndrome 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000327157 SCV000395779 uncertain significance Autosomal recessive pseudohypoaldosteronism type 1 2016-06-14 criteria provided, single submitter clinical testing

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