{{Rsnum
|rsid=2304682
|Gene=EMILIN1
|Chromosome=2
|position=27084901
|Orientation=minus
|GMAF=0.3338
|Gene_s=EMILIN1,KHK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 14.3 | 49.2 | 36.5
| HCB | 17.8 | 37.8 | 44.4
| JPT | 2.3 | 27.3 | 70.5
| YRI | 9.7 | 27.4 | 62.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 17.8 | 37.8 | 44.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| 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=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].
}}