ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.1903T>C (p.Cys635Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Medizinische Genetik Mainz RCV004545956 SCV005040935 uncertain significance 46,XY sex reversal 6 2022-05-18 criteria provided, single submitter clinical testing ACMG Criteria: PM2_SUP,PP3

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