ClinVar Miner

Submissions for variant NM_005996.4(TBX3):c.961dup (p.Ser321fs)

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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 RCV002289028 SCV002581374 likely pathogenic Ulnar-mammary syndrome 2022-02-23 criteria provided, single submitter clinical testing

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