Variant (rsID / SNP)
rs2308321
rs2308321 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MGMT. Location: chromosome 10, position 131,565,064. The table records no clinical significance for this variant.
Reference-table entries
MGMTNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:131565064
- HGVS
- NM_002412.5,c.427A>G,p.Ile143Val
- Allele change
- Missense_I174V
Associated conditions / phenotypes
Diffuse Large B-Cell Lymphoma|Lymphoma, Non-Hodgkin, Familial|Pancytopenia|Prostate Cancer|Neutropenia|Thrombocytopenia|Follicular Lymphoma|Myelodysplastic Syndrome|Lymphoma, Hodgkin, Classic|Glioma|Glioblastoma|B-Cell Lymphoma|Glial Tumor
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.