ClinVar Miner

Submissions for variant NM_001101362.3(KBTBD13):c.1309C>T (p.Gln437Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004813313 SCV005438101 uncertain significance Colorectal cancer, susceptibility to, 12 2024-12-17 criteria provided, single submitter clinical testing

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