ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.4102-1G>C

dbSNP: rs2081113293
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001252992 SCV001428488 likely pathogenic Intellectual disability, autosomal dominant 14 2018-11-05 criteria provided, single submitter clinical testing

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