ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.6101del (p.Leu2034fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289102 SCV002581557 likely pathogenic KBG syndrome 2022-06-21 criteria provided, single submitter clinical testing

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