ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.114GGC[6] (p.Ala45dup)

dbSNP: rs587779737
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000114252 SCV000147811 likely benign not specified 2016-03-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000946455 SCV001092591 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV000946455 SCV001818608 likely benign not provided 2020-09-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259599 SCV002539443 benign Intellectual disability, autosomal dominant 14 2021-12-05 criteria provided, single submitter clinical testing

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