ClinVar Miner

Submissions for variant NM_000888.5(ITGB6):c.871G>A (p.Gly291Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004760286 SCV005374458 uncertain significance Amelogenesis imperfecta type 1H 2024-09-22 criteria provided, single submitter clinical testing

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