List of variants in gene combination HBA2, LOC106804612 reported as benign for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000517.6(HBA2):c.-43G>C	rs71382271	1.00000
NM_000517.6(HBA2):c.*107A>G	rs2541640	0.99433
NM_000517.6(HBA2):c.-24C>G	rs772829778	0.06872
NM_000517.6(HBA2):c.300+55T>G	rs2362746	0.01848
NM_000517.6(HBA2):c.414C>T (p.Thr138=)	rs371394396	0.00001
NC_000016.10:g.172832C>A	rs1596569257
NM_000517.6(HBA2):c.245C>T (p.Ser82Phe)	rs281864864
NM_000517.6(HBA2):c.301-24delinsCTCGGCCC	rs1596570272
NM_000517.6(HBA2):c.95+11_95+34del	rs1445188229

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.