ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.1293_1311dup (p.Gly438fs)

dbSNP: rs943407609
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000722587 SCV002563927 pathogenic not provided 2021-04-01 criteria provided, single submitter clinical testing
Gharavi Laboratory, Columbia University RCV000722587 SCV000853718 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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