ClinVar Miner

Submissions for variant NM_031443.4(CCM2):c.205-11866_205-11863del

dbSNP: rs547206569
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics Greifswald, Research Division, University Medicine Greifswald RCV000591876 SCV000579373 not provided Cerebral cavernous malformation 2 2017-05-15 no assertion provided research

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