{{Rsnum
|rsid=13278732
|Gene=C8orf47
|Chromosome=8
|position=98076353
|Orientation=plus
|GMAF=0.1722
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ERICH5
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 51.8 | 41.1 | 7.1
| HCB | 89.1 | 10.9 | 0.0
| JPT | 95.6 | 4.4 | 0.0
| YRI | 53.4 | 42.5 | 4.1
| ASW | 57.9 | 36.8 | 5.3
| CHB | 89.1 | 10.9 | 0.0
| CHD | 89.0 | 11.0 | 0.0
| GIH | 60.4 | 35.6 | 4.0
| LWK | 60.6 | 34.9 | 4.6
| MEX | 63.8 | 36.2 | 0.0
| MKK | 59.6 | 30.8 | 9.6
| TSI | 55.9 | 38.2 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=T
|Pval=0.000006
|OR=1.31
|ORtxt=[1.04-1.65]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}