Variant (rsID / SNP)
rs4135113
rs4135113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TDG. Location: chromosome 12, position 104,376,693. The table records no clinical significance for this variant.
Reference-table entries
TDGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:104376693
- HGVS
- NM_003211.6,c.595G>A,p.Gly199Ser
- Allele change
- Missense_G56S
Associated conditions / phenotypes
Colorectal Cancer|Squamous Cell Carcinoma|Myelodysplastic Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.