ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.677-3C>T

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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 RCV003990366 SCV004806919 uncertain significance Hereditary lymphedema type I 2024-03-26 criteria provided, single submitter clinical testing

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