ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.2252-97A>T

dbSNP: rs113319329
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001616651 SCV001842057 benign not provided 2018-07-26 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260231 SCV002539463 benign Intellectual disability, autosomal dominant 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616651 SCV005284425 benign not provided criteria provided, single submitter not provided

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