ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.3524C>T (p.Pro1175Leu)

gnomAD frequency: 0.00003  dbSNP: rs145886877
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001582591 SCV001813281 likely benign not provided 2020-05-26 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 24728327)
Labcorp Genetics (formerly Invitae), Labcorp RCV001582591 SCV003483573 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
ITMI RCV000120060 SCV000084196 not provided not specified 2013-09-19 no assertion provided reference population

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