ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.1619C>T (p.Thr540Met)

gnomAD frequency: 0.00003  dbSNP: rs892173376
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
Genetic Services Laboratory, University of Chicago RCV000501414 SCV000593370 uncertain significance not specified 2017-03-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005056086 SCV005722247 benign not provided 2024-06-28 criteria provided, single submitter clinical testing

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