ClinVar Miner

Submissions for variant NM_000500.9(CYP21A2):c.292+9C>T

gnomAD frequency: 0.71669  dbSNP: rs6462
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251542 SCV000304548 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658180 SCV001876494 benign Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 2021-07-30 criteria provided, single submitter clinical testing

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