Variant (rsID / SNP)
rs675026
rs675026 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPRM1. Location: chromosome 6, position 154,414,563. Clinical significance in the table: drug_response.
Reference-table entries
OPRM1Drug response
- Clinical significance (as recorded)
- drug_response
- Variant type
- synonymous_variant
- Chromosome / position
- 6:154414563
- HGVS
- NM_001008505.2,c.1323A>G,p.Gly441Gly
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.