ClinVar Miner

List of variants in gene GALC reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_000153.4(GALC):c.1302C>T (p.Ser434=) rs3213918
NM_000153.4(GALC):c.1670+19A>T rs141839955
NM_000153.4(GALC):c.18C>G (p.Leu6=) rs886038260
NM_000153.4(GALC):c.195+19G>A rs189853941
NM_000153.4(GALC):c.329-10_329-8del rs770389075
NM_000153.4(GALC):c.443-12T>G rs886038261
NM_000153.4(GALC):c.443-30C>T rs886038262
NM_000153.4(GALC):c.60C>T (p.Ala20=) rs188488238

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.