ClinVar Miner

Variants studied for Rubinstein-Taybi syndrome 2

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 not provided total
27 10 7 1 0 2 47

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign not provided total
EP300 27 10 7 1 2 47

Submitter and significance breakdown #

Total submitters: 16
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Submitter pathogenic likely pathogenic uncertain significance likely benign not provided total
OMIM 9 0 0 0 0 9
Genetic Services Laboratory, University of Chicago 2 0 6 0 0 8
Fundacion Rioja Salud,Center for Biomedical Research (CIBIR) 7 0 0 0 0 7
Molecular Genetics Laboratory,BC Children's and BC Women's Hospitals 1 4 0 0 0 5
Baylor Genetics 1 1 1 0 0 3
Equipe Genetique des Anomalies du Developpement,Université de Bourgogne 1 2 0 0 0 3
Invitae 2 0 0 0 0 2
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 1 0 0 0 2
Centre de Biologie Pathologie Génétique,Centre Hospitalier Universitaire de Lille 1 0 0 1 0 2
SickKids Clinical Genetics Group,The Hospital for Sick Children 0 0 0 0 2 2
Mendelics 1 0 0 0 0 1
ITMI 1 0 0 0 0 1
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 1 0 0 0 1
Center of Genomic medicine, Geneva,University Hospital of Geneva 1 0 0 0 0 1
Center for Human Genetics,University of Leuven 0 1 0 0 0 1
Laboratory Genomica,Gynecology and Assisted Reproduction Hospital Malinov DM 1 0 0 0 0 1

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