ClinVar Miner

List of variants in gene SGCD reported as uncertain significance by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_000337.5(SGCD):c.193-12G>T rs727503421
NM_000337.5(SGCD):c.383-11A>T rs727504584
NM_000337.5(SGCD):c.4-12C>T rs727504580
NM_000337.5(SGCD):c.451T>G (p.Ser151Ala) rs121909298
NM_000337.5(SGCD):c.494G>A (p.Arg165Gln) rs727503423
NM_000337.5(SGCD):c.506C>T (p.Ala169Val) rs876658001
NM_000337.5(SGCD):c.697G>A (p.Glu233Lys) rs768979513
NM_000337.5(SGCD):c.699+72A>C rs376317697
NM_000337.5(SGCD):c.731C>T (p.Pro244Leu) rs375159661
NM_000337.5(SGCD):c.839C>A (p.Ser280Tyr) rs397516337
NM_000337.5(SGCD):c.92G>A (p.Arg31Gln) rs200476861

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.