ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.1066-31dup

dbSNP: rs35813860
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001527822 SCV001738960 benign not provided 2019-08-07 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465881 SCV002760515 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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