{{Rsnum
|rsid=9297216
|Chromosome=8
|position=34187743
|Orientation=plus
|GMAF=0.2231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 69.4 | 26.9 | 3.7
| HCB | 47.1 | 45.6 | 7.4
| JPT | 38.1 | 46.9 | 15.0
| YRI | 64.1 | 33.8 | 2.1
| ASW | 66.7 | 26.3 | 7.0
| CHB | 47.1 | 45.6 | 7.4
| CHD | 50.0 | 38.0 | 12.0
| GIH | 34.7 | 53.1 | 12.2
| LWK | 59.3 | 35.2 | 5.6
| MEX | 60.3 | 31.0 | 8.6
| MKK | 60.8 | 35.3 | 3.9
| TSI | 78.2 | 20.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23829686
  |Trait=Asthma (childhood onset)
  |Title=Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
  |RiskAllele=
  |Pval=1E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}