ClinVar Miner

Submissions for variant NM_000421.5(KRT10):c.1457_1458insAAGCT (p.His487fs)

dbSNP: rs762667965
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001530894 SCV001745801 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001530894 SCV002035038 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001530894 SCV002038383 uncertain significance not provided no assertion criteria provided clinical testing

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