ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.3199-95A>G

gnomAD frequency: 0.06005  dbSNP: rs76490152
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001725377 SCV001960324 benign not provided 2018-07-26 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260400 SCV002539467 benign Intellectual disability, autosomal dominant 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001725377 SCV005284428 benign not provided criteria provided, single submitter not provided

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