ClinVar Miner

Submissions for variant NM_016343.4(CENPF):c.3614_3617del (p.Ser1205fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV004547205 SCV005042568 likely pathogenic Stromme syndrome criteria provided, single submitter clinical testing

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