ClinVar Miner

Submissions for variant NM_001145358.2(SIN3A):c.942C>T (p.Ile314=)

gnomAD frequency: 0.00096  dbSNP: rs147885320
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000908933 SCV001053717 benign not provided 2024-01-17 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818809 SCV002064642 likely benign not specified 2019-07-03 criteria provided, single submitter clinical testing

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