List of variants in gene HBG2 reported as other

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000184.2(HBG2):c.439C>T (p.His147Tyr)	rs34807671	0.00001
NM_000184.2(HBG2):c.353A>G (p.His118Arg)	rs36049074
NM_000184.2(HBG2):c.355T>C (p.Phe119Leu)	rs35020253
NM_000184.2(HBG2):c.361A>C (p.Lys121Gln)	rs34703519
NM_000184.2(HBG2):c.364G>A (p.Glu122Lys)	rs63750021
NM_000184.2(HBG2):c.377A>C (p.Glu126Ala)	rs34997902
NM_000184.2(HBG2):c.391T>G (p.Trp131Gly)	rs35826780

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.