ClinVar Miner

Variants studied for Zellweger spectrum disorders

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
249 265 805 891 92 3 2191

Gene and significance breakdown #

Total genes and gene combinations: 9
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
PEX1 149 92 378 591 39 0 1173
GATAD1, PEX1 57 45 134 247 16 2 466
PEX6 15 62 149 15 19 0 260
PEX10 11 37 81 11 11 0 151
PEX2 4 23 48 5 5 0 85
LOC129998796, PEX1 13 3 15 22 1 0 51
PEX19 0 2 0 0 0 1 3
LOC129998796, PEX1, RBM48 0 0 0 0 1 0 1
PEX5 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 5
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 208 47 408 844 57 0 1564
Natera, Inc. 74 226 472 75 58 0 905
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 3 3
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 0 3 0 0 0 0 3
Genetics Institute, Tel Aviv Sourasky Medical Center 1 0 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. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.