Variant (rsID / SNP)
rs12917
rs12917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MGMT. Location: chromosome 10, position 131,506,283. The table records no clinical significance for this variant.
Reference-table entries
MGMTNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:131506283
- HGVS
- NM_002412.5,c.250C>T,p.Leu84Phe
- Allele change
- Missense_L115F
Associated conditions / phenotypes
Lymphoma, Hodgkin, Classic|Lymphoma|Glioma|Glial Tumor|Diffuse Large B-Cell Lymphoma|Follicular Lymphoma|B-Cell Lymphoma|Pancytopenia|Prostate Cancer|Neutropenia|Thrombocytopenia|Glioblastoma|Lymphoma, Non-Hodgkin, Familial|Squamous Cell Carcinoma|Gallbladder Disease 1|Colorectal Cancer|Myelodysplastic Syndrome|Gallbladder Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.