ClinVar Miner

Variants in gene PIGN with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
Download table as spreadsheet
HGVS dbSNP
NM_176787.5(PIGN):c.1617T>C (p.Tyr539=) rs147306123
NM_176787.5(PIGN):c.2238A>G (p.Ile746Met) rs200658159
NM_176787.5(PIGN):c.2577-13dup rs138671843
NM_176787.5(PIGN):c.2620-17dup rs11437076
NM_176787.5(PIGN):c.2620-5del rs11437076
NM_176787.5(PIGN):c.2751G>T (p.Thr917=) rs200481058
NM_176787.5(PIGN):c.528G>A (p.Thr176=) rs144304758

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.