Variant (rsID / SNP)
rs3821242
rs3821242 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A3. Location: chromosome 2, position 234,637,803. The table records no clinical significance for this variant.
Reference-table entries
UGT1A3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:234637803
- HGVS
- NM_019093.4,c.31T>C,p.Trp11Arg
- Allele change
- Silent
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.