ClinVar Miner

Submissions for variant NM_177550.5(SLC13A5):c.1157-68GT[22]

dbSNP: rs200900896
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001614454 SCV001833775 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072370 SCV002417598 benign Developmental and epileptic encephalopathy, 25 2025-02-03 criteria provided, single submitter clinical testing

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