ClinVar Miner

Submissions for variant NM_001039.4(SCNN1G):c.*597dup

dbSNP: rs566227302
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000351489 SCV000395768 likely benign Autosomal recessive pseudohypoaldosteronism type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000390316 SCV000395769 likely benign Liddle syndrome 1 2016-06-14 criteria provided, single submitter clinical testing

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