ClinVar Miner

Submissions for variant CYP21A2, GENE CONVERSION CYP21 FROM CYP21P

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000012945 SCV000033187 pathogenic Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 1988-01-01 no assertion criteria provided literature only

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