ClinVar Miner

Submissions for variant NM_003403.5(YY1):c.468_483del (p.Gly157fs)

dbSNP: rs1890695996
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001266005 SCV001444177 pathogenic Inborn genetic diseases 2019-11-21 criteria provided, single submitter clinical testing
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV001268245 SCV001447035 pathogenic not provided 2020-10-23 criteria provided, single submitter clinical testing

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