Variant (rsID / SNP)
rs28365063
rs28365063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT2B7. Location: chromosome 4, position 69,962,610. Clinical significance in the table: drug_response.
Reference-table entries
UGT2B7Drug response
- Clinical significance (as recorded)
- drug_response
- Variant type
- synonymous_variant
- Chromosome / position
- 4:69962610
- HGVS
- NM_001074.4,c.372A>G,p.Arg124Arg
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.