ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.2988+36G>A

gnomAD frequency: 0.00011  dbSNP: rs372175005
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656001 SCV001861711 benign not provided 2021-03-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260254 SCV002539466 benign Intellectual disability, autosomal dominant 14 2021-12-05 criteria provided, single submitter clinical testing

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