Variant (rsID / SNP)

rs2228079

rs2228079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADORA1. Location: chromosome 1, position 203,098,275. The table records no clinical significance for this variant.

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Reference-table entries

ADORA1Not classified

Variant type: synonymous_variant
Chromosome / position: 1:203098275
HGVS: NM_000674.3,c.306T>G,p.Ala102Ala
Allele change: Synonymous_A102A

Associated conditions / phenotypes

Attention Deficit-Hyperactivity Disorder|Obsessive-Compulsive Disorder|Gilles De La Tourette Syndrome|Tic Disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.