ClinVar Miner

Submissions for variant NM_016343.4(CENPF):c.1068G>A (p.Lys356=)

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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 RCV002289194 SCV002579052 uncertain significance Stromme syndrome 2022-04-04 criteria provided, single submitter clinical testing

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