Variant (rsID / SNP)
rs34079079
rs34079079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STT3A. Location: chromosome 11, position 125,482,982. Clinical significance in the table: Benign.
Reference-table entries
STT3ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:125482982
- Cytoband
- 11q24.2
- HGVS
- NM_152713.5(STT3A):c.1464T>C (p.Ile488=)
- Allele change
- Synonymous_I488I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.