List of variants reported as pathogenic for Hereditary spastic paraplegia by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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_003119.4(SPG7):c.1529C>T (p.Ala510Val)	rs61755320	0.00364
NM_025137.4(SPG11):c.1951C>T (p.Arg651Ter)	rs199588440	0.00002
NM_015346.4(ZFYVE26):c.6424C>T (p.Gln2142Ter)	rs1239601514	0.00001
NM_003119.4(SPG7):c.1053dup (p.Gly352fs)	rs760818649
NM_003119.4(SPG7):c.1450-1_1457del	rs768823392
NM_003119.4(SPG7):c.773_774del (p.Val258fs)	rs768136171
NM_025137.4(SPG11):c.3711dup (p.Tyr1238fs)	rs750663981
NM_025137.4(SPG11):c.6832_6833del (p.Ser2278fs)	rs312262784

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.