{{Rsnum
|rsid=964112
|Gene=ELP4
|Chromosome=11
|position=31657400
|Orientation=plus
|GMAF=0.3062
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ELP4
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 38.1 | 54.0 | 8.0
| HCB | 32.8 | 48.2 | 19.0
| JPT | 30.1 | 49.6 | 20.4
| YRI | 100.0 | 0.0 | 0.0
| ASW | 75.4 | 22.8 | 1.8
| CHB | 32.8 | 48.2 | 19.0
| CHD | 34.9 | 46.8 | 18.3
| GIH | 34.7 | 51.5 | 13.9
| LWK | 96.4 | 3.6 | 0.0
| MEX | 44.8 | 46.6 | 8.6
| MKK | 89.1 | 10.3 | 0.6
| TSI | 42.2 | 48.0 | 9.8
| HapMapRevision=28
}}[[rs964112]] 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=964112
}}

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}