ClinVar Miner

Submissions for variant NM_005555.4(KRT6B):c.332G>A (p.Gly111Asp) (rs61745883)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000602544 SCV000744722 benign Pachyonychia congenita 2 2015-08-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000602544 SCV000733180 benign Pachyonychia congenita 2 no assertion criteria provided clinical testing

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