ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.4751A>G (p.Gln1584Arg)

gnomAD frequency: 0.00008  dbSNP: rs558739370
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001654752 SCV001869135 benign not provided 2020-03-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001654752 SCV002350464 likely benign not provided 2025-01-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260260 SCV002539477 benign Intellectual disability, autosomal dominant 14 2021-12-05 criteria provided, single submitter clinical testing

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