ClinVar Miner

Variants studied for cerebral cavernous malformation 3

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
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If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
17 1 3 0 0 9 30

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance not provided total
PDCD10 17 1 3 9 30

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic likely pathogenic uncertain significance not provided total
Invitae 10 0 3 0 13
Institute of Human Genetics Greifswald, Research Division,University Medicine Greifswald 0 0 0 9 9
OMIM 7 0 0 0 7
Baylor Genetics 1 0 0 0 1
Hehr Laboratory,Center for Human Genetics - University of Regensburg 0 1 0 0 1

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