Variant (rsID / SNP)
rs5751876
rs5751876 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADORA2A. Location: chromosome 22, position 24,837,301. The table records no clinical significance for this variant.
Reference-table entries
ADORA2ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 22:24837301
- HGVS
- NM_000675.6,c.1083T>C,p.Tyr361Tyr
- Allele change
- Silent
Associated conditions / phenotypes
Attention Deficit-Hyperactivity Disorder|Obsessive-Compulsive Disorder|Gilles De La Tourette Syndrome|Tic Disorder|Clopidogrel Resistance|Myocardial Infarction|Gas Gangrene|Anxiety|Huntington Disease|Panic Disorder|Rheumatoid Arthritis|Myopia|Agoraphobia|Arthritis|Plasmodium Falciparum Malaria|Malaria|Headache|Interstitial Cystitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.