ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.1126C>T (p.Arg376Trp)

dbSNP: rs1018092020
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001837401 SCV002097989 uncertain significance Intellectual disability, autosomal dominant 14 2020-06-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002545212 SCV003288586 benign not provided 2024-01-25 criteria provided, single submitter clinical testing

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