ClinVar Miner

List of variants in gene WASHC5 studied for Spastic paraplegia, autosomal dominant

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014846.4(WASHC5):c.*40del	rs550928439	0.00074
NM_014846.4(WASHC5):c.269_270del	rs199912701
NM_014846.4(WASHC5):c.-124-11dup	rs886062656
NM_014846.4(WASHC5):c.3423+12_3423+15del	rs774994568

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.