{{Rsnum
|rsid=2172802
|Gene=LPHN3
|Chromosome=4
|position=61587491
|Orientation=plus
|GMAF=0.4421
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LPHN3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 50.4 | 43.4 | 6.2
| HCB | 12.6 | 43.7 | 43.7
| JPT | 14.4 | 51.4 | 34.2
| YRI | 27.2 | 46.9 | 25.9
| ASW | 28.1 | 52.6 | 19.3
| CHB | 12.6 | 43.7 | 43.7
| CHD | 16.7 | 50.9 | 32.4
| GIH | 48.0 | 43.0 | 9.0
| LWK | 41.3 | 45.9 | 12.8
| MEX | 22.2 | 50.0 | 27.8
| MKK | 35.3 | 49.4 | 15.4
| TSI | 61.4 | 32.7 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20522523
|Trait=Partial epilepsies
|Title=Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
|RiskAllele=
|Pval=0.000003
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}