{{Rsnum
|rsid=1324694
|Gene=ERLIN1
|Chromosome=10
|position=101946445
|Orientation=plus
|GMAF=0.07254
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 98.5 | 1.5 | 0.0
| HCB | 84.4 | 13.3 | 2.2
| JPT | 83.0 | 16.1 | 0.9
| YRI | 71.2 | 26.7 | 2.1
| ASW | 76.4 | 23.6 | 0.0
| CHB | 84.4 | 13.3 | 2.2
| CHD | 76.2 | 22.9 | 1.0
| GIH | 84.7 | 15.3 | 0.0
| LWK | 62.9 | 34.3 | 2.9
| 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
|PMID=20198315
|Title=Association of genetic variants with hemorrhagic stroke in Japanese individuals
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}