ClinVar Miner

Variants studied for autoimmune urticaria

Included ClinVar conditions (2):
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
3 0 220 102 53 375

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
PLCG2 3 220 102 53 375

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance likely benign benign total
Invitae 0 215 102 53 370
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 5 0 0 5
OMIM 3 0 0 0 3
Center for Precision Medicine,Vanderbilt University Medical Center 0 1 0 0 1
New York Genome Center 0 1 0 0 1

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