ClinVar Miner

Variants studied for atopic eczema

Included ClinVar conditions (9):
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 affects total
7 3 9 0 0 1 19

Gene and significance breakdown #

Total genes and gene combinations: 6
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Gene or gene combination pathogenic likely pathogenic uncertain significance affects total
FLG 7 2 3 0 11
CYP4F22 0 0 2 0 2
IL21R 0 0 2 0 2
IL4R 0 0 2 0 2
HAVCR1 0 0 0 1 1
KCNJ11 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance affects total
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 4 0 4
Baylor Genetics 1 1 1 0 3
Fulgent Genetics,Fulgent Genetics 3 0 0 0 3
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 1 2 0 3
Mayo Clinic Laboratories, Mayo Clinic 0 0 2 0 2
Knight Diagnostic Laboratories, Oregon Health and Sciences University 2 0 0 0 2
Undiagnosed Diseases Network,NIH 2 0 0 0 2
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 2 0 0 0 2
Institute for Genomic Medicine (IGM) Clinical Laboratory,Nationwide Children's Hospital 2 0 0 0 2
OMIM 0 0 0 1 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 1 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 1 0 0 1

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