{{Rsnum
|rsid=2289360
|Gene=EMILIN1
|Chromosome=2
|position=27079297
|Orientation=minus
|GMAF=0.404
|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 | 15.6 | 48.6 | 35.8
| HCB | 10.2 | 45.3 | 44.5
| JPT | 2.7 | 29.5 | 67.9
| YRI | 36.8 | 49.3 | 13.9
| ASW | 33.3 | 47.4 | 19.3
| CHB | 10.2 | 45.3 | 44.5
| CHD | 5.6 | 38.3 | 56.1
| GIH | 8.1 | 35.4 | 56.6
| LWK | 33.6 | 48.2 | 18.2
| MEX | 36.2 | 43.1 | 20.7
| MKK | 28.1 | 48.4 | 23.5
| TSI | 15.7 | 47.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=20186130
|Title=Association study of the elastin microfibril interfacer 1 (EMILIN1) gene in essential hypertension
}}

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

{{on chip | Illumina Human 1M}}