ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.908G>C (p.Ser303Thr)

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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 RCV005151149 SCV005776422 benign not provided 2024-04-22 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005358227 SCV005919685 uncertain significance Coffin-Siris syndrome 2021-07-30 criteria provided, single submitter research

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