Variant (rsID / SNP)
rs2228129
rs2228129 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLR2A. Location: chromosome 17, position 7,402,600. The table records no clinical significance for this variant.
Reference-table entries
POLR2ANot classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 17:7402600
- HGVS
- NM_000937.5,c.1461T>C,p.Ser487Ser
- Allele change
- Synonymous_S487S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.