ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.4721C>T (p.Pro1574Leu)

gnomAD frequency: 0.00006  dbSNP: rs370889837
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001667588 SCV001890121 benign not provided 2020-05-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001667588 SCV002419274 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing

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