ClinVar Miner

Variants from Bruce Budowle Laboratory, University of North Texas Health Science Center

Location: United States  Primary collection method: research
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 drug response total
0 0 0 0 0 1610 1610

Gene and significance breakdown #

Total genes and gene combinations: 17
Download table as spreadsheet
Gene or gene combination drug response total
ABCB1 567 567
OPRM1 453 453
CYP2D6 186 186
UGT2B7 120 120
COMT 71 71
CYP2D6, LOC110740340 49 49
ABCB1, RUNDC3B 23 23
ABCB1, LOC126860097 20 20
IPCEF1, OPRM1 13 13
LOC114803476, UGT2B7 9 9
COMT, LOC112694766 2 2
COMT, LOC130066960, TXNRD2 2 2
COMT, LOC130066961 2 2
COMT, LOC130066962 1 1
COMT, MIR4761 1 1

Condition and significance breakdown #

Total conditions: 1
Download table as spreadsheet
Condition drug response total
Tramadol response 1610 1610

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.