Variant (rsID / SNP)

rs3825413

rs3825413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLITRK6. Location: chromosome 13, position 86,369,120. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLITRK6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:86369120
Cytoband: 13q31.1
HGVS: NM_032229.3(SLITRK6):c.1524G>A (p.Leu508=)
Allele change: Synonymous_L508L

Associated conditions / phenotypes

High myopia-sensorineural deafness 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.