{{Rsnum
|rsid=2292096
|Gene=CAMSAP1L1
|Chromosome=1
|position=200857641
|Orientation=plus
|GMAF=0.1515
|Gene_s=CAMSAP1L1
|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 | 77.7 | 19.6 | 2.7
| HCB | 58.4 | 38.7 | 2.9
| JPT | 73.9 | 25.2 | 0.9
| YRI | 64.1 | 34.5 | 1.4
| ASW | 64.9 | 31.6 | 3.5
| CHB | 58.4 | 38.7 | 2.9
| CHD | 65.1 | 33.9 | 0.9
| GIH | 80.2 | 16.8 | 3.0
| LWK | 70.4 | 28.7 | 0.9
| MEX | 70.7 | 24.1 | 5.2
| MKK | 83.2 | 15.5 | 1.3
| TSI | 82.4 | 17.6 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22116939
|Trait=None
|Title=Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
|RiskAllele=
|Pval=1E-8
|OR=1.5900
|ORtxt=None
}}

{{PMID Auto
|PMID=24148305
|Title=The potential role of CAMSAP1L1 in symptomatic epilepsy
}}

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