ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.4304A>G (p.Tyr1435Cys)

gnomAD frequency: 0.00026  dbSNP: rs369118235
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001657755 SCV001872603 benign not provided 2019-05-31 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 24728327)
Invitae RCV001657755 SCV003275677 benign not provided 2024-01-02 criteria provided, single submitter clinical testing
ITMI RCV000120062 SCV000084198 not provided not specified 2013-09-19 no assertion provided reference population

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