Variant (rsID / SNP)
rs457705
rs457705 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETS2. Location: chromosome 21, position 40,191,431. The table records no clinical significance for this variant.
Reference-table entries
ETS2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:40191431
- HGVS
- NM_001256295.2,c.1236T>G,p.Thr412Thr
- Allele change
- Synonymous_T412T
Associated conditions / phenotypes
Oral Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.