{{Rsnum
|rsid=11031434
|Gene=ELP4
|Chromosome=11
|position=31631665
|Orientation=plus
|GMAF=0.3949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ELP4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.1 | 53.1 | 32.8
| HCB | 43.2 | 43.2 | 13.6
| JPT | 33.3 | 53.3 | 13.3
| YRI | 1.6 | 8.1 | 90.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 43.2 | 43.2 | 13.6
| 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
}}[[rs11031434]] is a SNP in the elongator protein complex 4 [[ELP4]] gene.

* Associated with rolandic [[epilepsy]], as part of a relatively tightly linked cluster of 3 SNPs ([[rs964112]], [[rs11031434]], and [[rs986527]].{{Doi|10.1038/ejhg.2008.267}}

{{omim
|id=117100
|rsnum=11031434
}}

{{PMID|19172991|OA=1
}} Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}