ClinVar Miner

Variants in gene PLA2G7

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 risk factor not provided total
2 3 62 17 6 2 2 88

Condition and significance breakdown #

Total conditions: 5
Download table as spreadsheet
Condition pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
not specified 0 0 56 14 0 0 0 70
Platelet-activating factor acetylhydrolase deficiency 2 3 5 0 0 2 0 10
not provided 0 0 2 2 4 0 2 9
PLA2G7-related disorder 0 0 2 2 4 0 0 8
RECLASSIFIED - MYOC POLYMORPHISM 0 0 0 0 2 0 0 2

Submitter and significance breakdown #

Total submitters: 14
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
Ambry Genetics 0 0 49 6 0 0 0 55
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 2 9 8 0 0 0 19
PreventionGenetics, part of Exact Sciences 0 0 0 2 4 0 0 6
OMIM 2 0 0 0 2 0 0 4
GeneDx 0 0 1 0 3 0 0 4
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 4 0 0 0 0 4
Labcorp Genetics (formerly Invitae), Labcorp 0 0 0 2 1 0 0 3
Lab. of Molecular Biology of Arterial Hypertension University of Padova 0 0 0 0 0 0 2 2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 1 1 0 0 0 0 2
Reproductive Health Research and Development, BGI Genomics 0 0 0 0 0 2 0 2
Baylor Genetics 0 1 0 0 0 0 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 0 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 0 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 0 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.