{{Rsnum
|rsid=10906189
|Gene=CAMK1D
|Chromosome=10
|position=12675061
|Orientation=plus
|GMAF=0.4959
|Gene_s=CAMK1D
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.4 | 46.9 | 25.7
| HCB | 13.1 | 52.6 | 34.3
| JPT | 13.3 | 58.4 | 28.3
| YRI | 25.2 | 45.6 | 29.3
| ASW | 26.3 | 52.6 | 21.1
| CHB | 13.1 | 52.6 | 34.3
| CHD | 18.5 | 43.5 | 38.0
| GIH | 32.7 | 47.5 | 19.8
| LWK | 29.4 | 47.7 | 22.9
| MEX | 19.0 | 50.0 | 31.0
| MKK | 42.9 | 47.4 | 9.6
| TSI | 28.4 | 50.0 | 21.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23459443
  |Trait=QT interval (interaction)
  |Title=Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
  |RiskAllele=A
  |Pval=6E-6
  |OR=NR
  |ORtxt=NR
  }}

{{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}}