{{Rsnum
|rsid=989554
|Gene=ERG
|Chromosome=21
|position=38415005
|Orientation=plus
|GMAF=0.2043
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ERG
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 77.0 | 21.2 | 1.8
| HCB | 67.2 | 28.5 | 4.4
| JPT | 55.8 | 38.1 | 6.2
| YRI | 41.1 | 47.3 | 11.6
| ASW | 63.2 | 35.1 | 1.8
| CHB | 67.2 | 28.5 | 4.4
| CHD | 61.5 | 31.2 | 7.3
| GIH | 88.1 | 11.9 | 0.0
| LWK | 50.9 | 40.9 | 8.2
| MEX | 65.5 | 32.8 | 1.7
| MKK | 52.6 | 39.1 | 8.3
| TSI | 72.5 | 22.5 | 4.9
| HapMapRevision=28
}}

Part of a [[haplotype]] linked to [[stroke]] affecting perhaps 5% of [[sickle cell anemia patients]]

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}