ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.4843G>A (p.Gly1615Ser)

dbSNP: rs1274057762
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503583 SCV000593411 likely benign not specified 2017-11-16 criteria provided, single submitter clinical testing

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