{{Rsnum
|rsid=6660197
|Chromosome=1
|position=200734413
|Orientation=plus
|GMAF=0.146
|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 | 77.0 | 20.4 | 2.7
| HCB | 56.9 | 38.7 | 4.4
| JPT | 73.5 | 23.9 | 2.7
| YRI | 68.7 | 29.9 | 1.4
| ASW | 66.7 | 29.8 | 3.5
| CHB | 56.9 | 38.7 | 4.4
| CHD | 64.2 | 34.9 | 0.9
| GIH | 81.2 | 15.8 | 3.0
| LWK | 80.0 | 20.0 | 0.0
| MEX | 70.7 | 24.1 | 5.2
| MKK | 94.2 | 5.8 | 0.0
| TSI | 83.3 | 16.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22116939
|Title=Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}