Variants in gene combination HBB, LOC107133510, LOC110006319 with conflicting interpretations reported as "likely benign and "other"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (other) minimum review status:		Submission 2 (other) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.389C>T (p.Ala130Val)	rs111645889	0.00007
NM_000518.5(HBB):c.380T>C (p.Val127Ala)	rs33925391	0.00001
NM_000518.5(HBB):c.394C>A (p.Gln132Lys)	rs33910209
NM_000518.5(HBB):c.394C>G (p.Gln132Glu)	rs33910209
NM_000518.5(HBB):c.397A>C (p.Lys133Gln)	rs33953406
NM_000518.5(HBB):c.420T>A (p.Asn140Lys)	rs34240441

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.