{{Rsnum
|rsid=2011616
|Gene=EMILIN1
|Chromosome=2
|position=27079693
|Orientation=plus
|GMAF=0.3462
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=EMILIN1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 17.7 | 45.1 | 37.2
| HCB | 10.9 | 45.3 | 43.8
| JPT | 2.7 | 25.7 | 71.7
| YRI | 3.4 | 38.8 | 57.8
| ASW | 5.3 | 56.1 | 38.6
| CHB | 10.9 | 45.3 | 43.8
| CHD | 5.5 | 40.4 | 54.1
| GIH | 9.9 | 36.6 | 53.5
| LWK | 8.2 | 44.5 | 47.3
| MEX | 34.5 | 41.4 | 24.1
| MKK | 17.3 | 56.4 | 26.3
| TSI | 16.7 | 49.0 | 34.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=20186130
|Title=Association study of the elastin microfibril interfacer 1 (EMILIN1) gene in essential hypertension
}}

{{PMID Auto
|PMID=22639547
|Title=Pooled Analyses of the Associations of Polymorphisms in the GRK4 and EMILIN1 Genes with Hypertension Risk
|OA=1
}}

{{PMID Auto
|PMID=19922630
|Title=Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population.
|OA=1
}}

{{PMID Auto
|PMID=21462127
|Title=[Association of EMILIN1 gene polymorphism with essential hypertension in Mongolian].
}}

{{PMID Auto
|PMID=21753788
|Title=Association of intronic single-nucleotide polymorphisms in the EMILIN1 gene with essential hypertension in a Chinese population.
}}

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