ClinVar Miner

List of variants in gene IGH, IGHM studied for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000014.9:g.105855041A>G rs10287 0.05231
NC_000014.9:g.105855988G>C rs113762053 0.04825
NC_000014.9:g.105854900G>T rs373184157 0.00003
NC_000014.9:g.105854405C>T rs376256147 0.00002
NC_000014.9:g.105854468A>C rs267606871
NC_000014.9:g.105855107C>T rs281865422
NC_000014.9:g.105855132dup rs2092930640
NC_000014.9:g.105855203G>A
NC_000014.9:g.105855623_105855624del
NC_000014.9:g.105856013G>T rs2142904095
NC_000014.9:g.105856087G>A rs2142904392
NC_000014.9:g.105856156C>T rs201981439

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.