ClinVar Miner

Submissions for variant NM_000356.4(TCOF1):c.1722T>C (p.Thr574=) (rs151344571)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics Laboratories, Oxford Radcliffe Hospitals NHS Trust RCV000190972 SCV000245859 likely benign Treacher Collins syndrome 1 no assertion criteria provided not provided

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