ClinVar Miner

Submissions for variant NM_000500.9(CYP21A2):c.17_19TGC[6] (p.Leu10dup) (rs61338903)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000024070 SCV000045361 benign 21-HYDROXYLASE POLYMORPHISM 1987-06-01 no assertion criteria provided literature only
GeneReviews RCV000055814 SCV000086794 non-pathogenic Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 2013-08-29 no assertion criteria provided curation Converted during submission to Benign.

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