ClinVar Miner

Submissions for variant NM_182977.3(NNT):c.-26T>C

gnomAD frequency: 0.23678  dbSNP: rs12187908
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001785445 SCV002026822 benign Glucocorticoid deficiency 4 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716812 SCV005298751 benign not provided criteria provided, single submitter not provided

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