ClinVar Miner

List of variants in gene RHAG reported as pathogenic for Rh-null, regulator type

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_000324.2(RHAG):c.1067+1G>A rs1562012617
NM_000324.2(RHAG):c.1086del (p.Ala363fs) rs1562011389
NM_000324.2(RHAG):c.1139G>T (p.Gly380Val) rs121918589
NM_000324.2(RHAG):c.154_157delinsGA (p.Pro52fs) rs387906519
NM_000324.2(RHAG):c.157+1G>A rs375508949
NM_000324.2(RHAG):c.836G>A (p.Gly279Glu) rs121918587
NM_000324.2(RHAG):c.946-1G>A rs1562012697

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.