Variant (rsID / SNP)
rs702764
rs702764 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPRK1. Location: chromosome 8, position 54,142,157. The table records no clinical significance for this variant.
Reference-table entries
OPRK1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 8:54142157
- HGVS
- NM_001318497.2,c.843A>G,p.Ala281Ala
- Allele change
- Synonymous_A281A
Associated conditions / phenotypes
Novelty Seeking Personality Trait|Opioid Addiction|Neonatal Abstinence Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.