Variant (rsID / SNP)
rs6706232
rs6706232 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A3. Location: chromosome 2, position 234,637,853. The table records no clinical significance for this variant.
Reference-table entries
UGT1A3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:234637853
- HGVS
- NM_019093.4,c.81G>A,p.Glu27Glu
- Allele change
- Silent
Associated conditions / phenotypes
Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.