List of variants in gene SLITRK1 reported as likely benign for Tourette syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001281503.2(SLITRK1):c.*2042T>A	rs1046202	0.27902
NM_001281503.2(SLITRK1):c.*801A>C	rs9593836	0.06546
NM_001281503.2(SLITRK1):c.*1160G>A	rs9602286	0.05824
NM_001281503.2(SLITRK1):c.*1134T>C	rs3737193	0.02647
NM_001281503.2(SLITRK1):c.-53-217T>C	rs74099450	0.01128
NM_001281503.2(SLITRK1):c.*649A>G	rs57857456	0.00623
NM_001281503.2(SLITRK1):c.*1963C>T	rs117206130	0.00124
NM_001281503.2(SLITRK1):c.988T>G (p.Ser330Ala)	rs145628951	0.00078
NM_001281503.2(SLITRK1):c.*2043del	rs66938370

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.