ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1672C>A (p.Arg558=)

dbSNP: rs372264472
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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 RCV001819544 SCV002068672 uncertain significance not specified 2021-08-24 criteria provided, single submitter clinical testing
Invitae RCV002074313 SCV002387476 likely benign Fanconi anemia 2023-02-11 criteria provided, single submitter clinical testing

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