Variant (rsID / SNP)
rs1045280
rs1045280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARRB2. Location: chromosome 17, position 4,622,638. The table records no clinical significance for this variant.
Reference-table entries
ARRB2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:4622638
- HGVS
- NM_001257328.2,c.903C>T,p.Ser301Ser
- Allele change
- Silent
Associated conditions / phenotypes
Tardive Dyskinesia|Schizophrenia|Alzheimer Disease|Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Parkinsonism|Schizophrenia 3|Cocaine Dependence|Opioid Addiction|Drug Dependence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.