ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.3235+38C>T

gnomAD frequency: 0.08126  dbSNP: rs9384530
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001610392 SCV001837542 benign not provided 2018-08-10 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000114268 SCV000147827 likely benign not specified no assertion criteria provided clinical testing Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.

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