ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.1631_1639del (p.Gly544_Ala546del)

dbSNP: rs1392865152
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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 RCV002982251 SCV003287579 likely benign not provided 2023-12-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003138422 SCV003826946 uncertain significance Coffin-Siris syndrome 1 2022-08-01 criteria provided, single submitter clinical testing

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