{{Rsnum
|rsid=4569005
|Gene=NELL1
|Chromosome=11
|position=21037185
|Orientation=plus
|GMAF=0.1552
|Gene_s=NELL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 68.1 | 30.1 | 1.8
| HCB | 95.6 | 4.4 | 0.0
| JPT | 91.2 | 8.8 | 0.0
| YRI | 46.9 | 44.9 | 8.2
| ASW | 44.6 | 48.2 | 7.1
| CHB | 95.6 | 4.4 | 0.0
| CHD | 93.6 | 6.4 | 0.0
| GIH | 58.4 | 32.7 | 8.9
| LWK | 47.3 | 45.5 | 7.3
| MEX | 77.6 | 22.4 | 0.0
| MKK | 42.3 | 42.3 | 15.4
| TSI | 70.6 | 25.5 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22379998
|Trait=None
|Title=Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.
|RiskAllele=
|Pval=0.000005
|OR=None
|ORtxt=None
|OA=1
}}

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