Variant (rsID / SNP)
rs3803739
rs3803739 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBE2O. Location: chromosome 17, position 74,387,284. The table records no clinical significance for this variant.
Reference-table entries
UBE2ONot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:74387284
- HGVS
- NM_022066.4,c.3619G>A,p.Gly1207Ser
- Allele change
- Missense_G1207S
Associated conditions / phenotypes
Colorectal Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.