ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.3978GCA[10] (p.Gln1333_Gln1334dup)

dbSNP: rs374564889
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501311 SCV000593364 likely benign not specified 2016-12-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496938 SCV002804592 likely benign Intellectual disability, autosomal dominant 14 2022-04-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002527201 SCV003288453 likely benign not provided 2023-11-18 criteria provided, single submitter clinical testing

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