{{Rsnum
|rsid=11191692
|Gene=CALHM1
|Chromosome=10
|position=105213765
|Orientation=plus
|GMAF=0.2828
|Gene_s=CALHM1,CALHM2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.0 | 46.9 | 38.1
| HCB | 10.2 | 39.4 | 50.4
| JPT | 9.7 | 51.3 | 38.9
| YRI | 0.0 | 4.1 | 95.9
| ASW | 0.0 | 17.5 | 82.5
| CHB | 10.2 | 39.4 | 50.4
| CHD | 8.3 | 38.5 | 53.2
| GIH | 27.7 | 51.5 | 20.8
| LWK | 3.6 | 17.3 | 79.1
| MEX | 13.8 | 46.6 | 39.7
| MKK | 2.6 | 23.1 | 74.4
| TSI | 18.6 | 56.9 | 24.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=24326043
|Title=No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population
}}

{{PMID Auto
|PMID=21439911
|Title=A polymorphism in CALHM1 is associated with temporal lobe epilepsy.
}}

{{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}}