ClinVar Miner

List of variants in gene GPD1L reported as benign for Brugada syndrome

Included ClinVar conditions (33):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_015141.3(GPD1L):c.366+8G>A rs72546650
NM_015141.3(GPD1L):c.396G>A (p.Lys132=) rs61741845
NM_015141.3(GPD1L):c.408C>T (p.Asp136=) rs9835387
NM_015141.3(GPD1L):c.465C>T (p.Ala155=) rs113645050
NM_015141.3(GPD1L):c.573C>G (p.Thr191=) rs72558073
NM_015141.3(GPD1L):c.619-9C>G rs2044880
NM_015141.3(GPD1L):c.813G>T (p.Arg271=) rs35464343
NM_015141.3(GPD1L):c.81T>C (p.Asn27=) rs34278284
NM_015141.3(GPD1L):c.828C>T (p.Ala276=) rs200392121
NM_015141.3(GPD1L):c.981G>A (p.Val327=) rs144877595
NM_015141.4(GPD1L):c.370A>G (p.Ile124Val) rs72552293

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.