ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.1791+6C>T

gnomAD frequency: 0.00001  dbSNP: rs1204011572
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002200053 SCV002359195 benign not provided 2024-10-17 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004531294 SCV004712430 likely benign ARID1B-related disorder 2021-08-06 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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