ClinVar Miner

Submissions for variant NM_000901.4(NR3C2):c.-275C>T

gnomAD frequency: 0.00187  dbSNP: rs61760022
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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 RCV000386990 SCV000447688 likely benign Autosomal dominant pseudohypoaldosteronism type 1 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710980 SCV005256217 likely benign not provided criteria provided, single submitter not provided

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