{{Rsnum
|rsid=16921914
|Gene=LOC100505848
|Chromosome=11
|position=31189224
|Orientation=plus
|GMAF=0.2309
|Gene_s=LOC100508736
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.3 | 41.6 | 53.1
| HCB | 15.6 | 45.9 | 38.5
| JPT | 14.2 | 48.7 | 37.2
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 14.0 | 86.0
| CHB | 15.6 | 45.9 | 38.5
| CHD | 13.8 | 45.9 | 40.4
| GIH | 9.9 | 47.5 | 42.6
| LWK | 0.0 | 2.7 | 97.3
| MEX | 8.6 | 39.7 | 51.7
| MKK | 0.0 | 7.7 | 92.3
| TSI | 5.0 | 30.7 | 64.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19801982
|Trait=Bone mineral density (spine)
|Title=Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
|RiskAllele=A
|Pval=2E-9
|OR=0.08
|ORtxt=[0.05-0.11] sd increase
|OA=1
}}

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs16921914
|overall_frequency_n=32
|overall_frequency_d=128
|overall_frequency=0.25
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=23
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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