ClinVar Miner

List of variants in gene SPG7 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_003119.3(SPG7):c.1807G>A (p.Ala603Thr) rs370852816
NM_003119.3(SPG7):c.2254C>G (p.His752Asp) rs1555618072
NM_003119.3(SPG7):c.2275G>A (p.Ala759Thr) rs140769107
NM_003119.3(SPG7):c.331A>G (p.Lys111Glu) rs1239421989
NM_003119.3(SPG7):c.4G>A (p.Ala2Thr) rs535030441
NM_003119.3(SPG7):c.53G>T (p.Gly18Val) rs1371729405

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.