ClinVar Miner

Submissions for variant NM_001366722.1(GRIP1):c.1331A>G (p.Lys444Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005004969 SCV005629679 uncertain significance Fraser syndrome 3 2024-06-08 criteria provided, single submitter clinical testing

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