Variant (rsID / SNP)
rs2228128
rs2228128 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLR2A. Location: chromosome 17, position 7,400,815. The table records no clinical significance for this variant.
Reference-table entries
POLR2ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:7400815
- HGVS
- NM_000937.5,c.960T>C,p.Asn320Asn
- Allele change
- Synonymous_N320N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
