ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.407C>T (p.Ser136Leu)

gnomAD frequency: 0.00005  dbSNP: rs1484818039
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001652185 SCV001866848 benign not provided 2019-07-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001652185 SCV002143625 likely benign not provided 2022-11-15 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001652185 SCV002497479 uncertain significance not provided 2022-01-01 criteria provided, single submitter clinical testing

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