ClinVar Miner

Variants studied for Brooke-Spiegler syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

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 total
33 0 45 37 6 121

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
CYLD 33 45 37 6 121

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 39 37 6 82
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia 23 6 0 0 29
OMIM 11 0 0 0 11

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