Variant (rsID / SNP)
rs9937
rs9937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRM1. Location: chromosome 11, position 4,159,457. The table records no clinical significance for this variant.
Reference-table entries
RRM1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:4159457
- HGVS
- NM_001033.5,c.2223A>G,p.Thr741Thr
- Allele change
- Synonymous_T741T
Associated conditions / phenotypes
Mucositis|Leukemia|Thrombocytopenia|Leukemia, Acute Myeloid|Toxic Encephalopathy|Myeloid Leukemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.