ClinVar Miner

Submissions for variant NM_024570.4(RNASEH2B):c.845C>T (p.Ala282Val)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine RCV003127449 SCV003804032 uncertain significance Autism spectrum disorder 2022-08-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004696311 SCV005192150 uncertain significance not provided criteria provided, single submitter not provided

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