Variant (rsID / SNP)

rs3737193

rs3737193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLITRK1. Location: chromosome 13, position 84,452,418. Clinical significance in the table: Likely benign.

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Reference-table entries

SLITRK1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:84452418
Cytoband: 13q31.1
HGVS: NM_001281503.2(SLITRK1):c.*1134T>C
Allele change: Silent

Associated conditions / phenotypes

Tourette syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.