{{Rsnum
|rsid=7807274
|Gene=MKLN1
|Chromosome=7
|position=131336340
|Orientation=plus
|GMAF=0.03719
|Gene_s=MKLN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 1.8 | 98.2
| YRI | 2.7 | 31.3 | 66.0
| ASW | 3.6 | 21.8 | 74.5
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 1.8 | 27.3 | 70.9
| MEX | 0.0 | 3.5 | 96.5
| MKK | 1.3 | 19.9 | 78.8
| TSI | 0.0 | 0.0 | 0.0
| 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=4E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{on chip | Affy GenomeWide 6}}