ClinVar Miner

Submissions for variant NM_001386125.1(OBSCN):c.11362C>A (p.Pro3788Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003414879 SCV004125958 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing OBSCN: BP4

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