ClinVar Miner

Submissions for variant NM_014159.7(SETD2):c.6110-27_6110-26del

dbSNP: rs10589946
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503779 SCV000597002 likely benign not specified 2016-04-29 criteria provided, single submitter clinical testing
GeneDx RCV001683530 SCV001900600 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002270595 SCV002555386 benign Luscan-Lumish syndrome 2022-03-15 criteria provided, single submitter clinical testing

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