ClinVar Miner

List of variants reported as benign for Lymphoproliferative disorder

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001167.4(XIAP):c.*5505del rs111508332 0.24545
NM_001167.4(XIAP):c.*5068_*5069insT rs58114044 0.15926
NM_001167.4(XIAP):c.*2296_*2300del rs79291374
NM_001167.4(XIAP):c.*3702dup rs762141177
NM_001167.4(XIAP):c.*4309dup rs397713705
NM_001167.4(XIAP):c.*5047del rs368295939
NM_001167.4(XIAP):c.*5180del rs60841987
NM_001167.4(XIAP):c.*5180dup rs60841987
NM_001167.4(XIAP):c.*5519del rs374013599
NM_002351.5(SH2D1A):c.*203del rs67202578

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.