ClinVar Miner

Variants in gene ACRBP

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
1 0 66 3 0 13 83

Condition and significance breakdown #

Total conditions: 17
Download table as spreadsheet
Condition pathogenic uncertain significance likely benign not provided total
not specified 0 66 3 0 69
Acute myeloid leukemia 0 0 0 3 3
Cervical cancer 0 0 0 2 2
Familial cancer of breast 0 0 0 2 2
Malignant lymphoma, large B-cell, diffuse 0 0 0 2 2
Malignant tumor of esophagus 0 0 0 2 2
Gastric cancer 0 0 0 1 1
Lung cancer 0 0 0 1 1
Lymphoma 0 0 0 1 1
Malignant tumor of urinary bladder 0 0 0 1 1
Neoplasm of brain 1 0 0 0 1
Nonpapillary renal cell carcinoma 0 0 0 1 1
Sarcoma 0 0 0 1 1
Thymoma 0 0 0 1 1
Thyroid cancer, nonmedullary, 1 0 0 0 1 1
Uterine corpus endometrial carcinoma 0 0 0 1 1
Uveal melanoma 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 3
Download table as spreadsheet
Submitter pathogenic uncertain significance likely benign not provided total
Ambry Genetics 0 66 3 0 69
Dr. Peter K. Rogan Lab, Western University 0 0 0 13 13
Department of Neurosurgery, Guangxi Colleges and Universities Key Laboratory of Preclinical Medicine Research 1 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.