ClinVar Miner

Variants studied for Short stature, optic nerve atrophy, and Pelger-Huet anomaly; Infantile liver failure 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
1 2 0 0 0 1 4

Gene and significance breakdown #

Total genes and gene combinations: 1
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic not provided total
NBAS 1 2 1 4

Submitter and significance breakdown #

Total submitters: 4
Download table as spreadsheet
Submitter pathogenic likely pathogenic not provided total
Clinical Genomics Program, Stanford Medicine 0 1 0 1
Division of Biology and Genetics,University of Brescia 0 1 0 1
Department of Pediatrics,Asahikawa Medical University 1 0 0 1
GenomeConnect - Invitae Patient Insights Network 0 0 1 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.