Variant (rsID / SNP)
rs61754380
rs61754380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYR. Location: chromosome 11, position 88,924,532. The table records no clinical significance for this variant.
Reference-table entries
TYRNot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:88924532
- Cytoband
- 11q14.3
- HGVS
- NM_000372.5(TYR):c.982G>C (p.Glu328Gln)
- Allele change
- Missense_E328Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.