List of variants reported as benign for Galactosemia

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

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.378-27G>C	rs41274865	0.04615
NM_000155.4(GALT):c.508-24G>A	rs41274867	0.04612
NM_000155.4(GALT):c.507+62G>A	rs2277202	0.04610
NM_000155.4(GALT):c.945T>C (p.His315=)	rs61735982	0.03311
NM_000155.4(GALT):c.876G>A (p.Thr292=)	rs1055607	0.02790
NM_000155.4(GALT):c.879C>T (p.Ser293=)	rs115527942	0.00407
NM_000155.4(GALT):c.510C>A (p.Ile170=)	rs61735984	0.00290
NM_000155.4(GALT):c.508-17G>A	rs12000481

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.