ClinVar Miner

Submissions for variant NM_000500.9(CYP21A2):c.318G>A (p.Pro106=)

dbSNP: rs6455
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248904 SCV000304553 likely benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics RCV000248904 SCV001143690 benign not specified 2020-09-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705079 SCV005225561 likely benign not provided criteria provided, single submitter not provided

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