Variant (rsID / SNP)
rs183484
rs183484 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRM1. Location: chromosome 11, position 4,141,132. The table records no clinical significance for this variant.
Reference-table entries
RRM1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:4141132
- HGVS
- NM_001033.5,c.850C>A,p.Arg284Arg
- Allele change
- Synonymous_R284R
Associated conditions / phenotypes
Leukemia|Leukemia, Acute Myeloid|Myeloid Leukemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.