ClinVar Miner

Submissions for variant NM_000497.3(CYP11B1):c.606G>A (p.Leu202=) (rs61751154)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000272874 SCV000472360 likely benign Congenital adrenal hyperplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000320919 SCV000472361 likely benign Hyperaldosteronism, familial, type I 2016-06-14 criteria provided, single submitter clinical testing

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