{{Rsnum
|rsid=7529251
|Gene=RYR2
|Chromosome=1
|position=237435116
|Orientation=plus
|GMAF=0.1896
|Gene_s=RYR2
|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 | 84.1 | 14.3 | 1.6
| HCB | 90.9 | 9.1 | 0.0
| JPT | 70.7 | 29.3 | 0.0
| YRI | 13.3 | 50.0 | 36.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 90.9 | 9.1 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=3E-7
  |OR=.28
  |ORtxt=[0.17-0.38] unit decrease
  |OA=1
}}

{{on chip | HumanOmni1Quad}}