ClinVar Miner

Variants studied for Levy-Hollister syndrome

Coded as:
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
8 9 5 5 0 27

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
FGFR2 4 3 2 4 13
FGF10 2 6 3 1 12
FGFR3 2 0 0 0 2

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
Center for Human Genetics, Inc, Center for Human Genetics, Inc 1 8 1 0 10
Illumina Laboratory Services, Illumina 0 0 3 5 8
OMIM 5 0 0 0 5
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 0 0 0 1
Dental Genetics Laboratory, Seoul National University School of Dentistry 1 0 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 1 0 0 1

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