Variant (rsID / SNP)
rs8133052
rs8133052 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBR3. Location: chromosome 21, position 37,507,501. The table records no clinical significance for this variant.
Reference-table entries
CBR3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 21:37507501
- HGVS
- NM_001236.4,c.11G>A,p.Cys4Tyr
- Allele change
- Silent
Associated conditions / phenotypes
Mucositis|Leukemia|Thrombocytopenia|Leukemia, Acute Myeloid|Myeloid Leukemia|Neutropenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.