ClinVar Miner

Submissions for variant NM_007217.4(PDCD10):c.-117+1010C>T

gnomAD frequency: 0.00005  dbSNP: rs912904786
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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 RCV000593756 SCV000579388 not provided Cerebral cavernous malformation 3 2017-05-15 no assertion provided research

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