ClinVar Miner

Submissions for variant NM_000102.4(CYP17A1):c.*165dup

dbSNP: rs45455494
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000285334 SCV000360134 uncertain significance Congenital adrenal hyperplasia 2016-06-14 criteria provided, single submitter clinical testing

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