ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.6196A>T (p.Asn2066Tyr)

dbSNP: rs1570622663
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000986282 SCV001135225 likely pathogenic Intellectual disability, autosomal dominant 14 2019-05-28 criteria provided, single submitter clinical testing

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