{{Rsnum
|rsid=9315385
|Gene=DCLK1
|Chromosome=13
|position=36089165
|Orientation=plus
|GMAF=0.2365
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=DCLK1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 1.8 | 26.5 | 71.7
| HCB | 19.7 | 47.4 | 32.8
| JPT | 17.7 | 38.9 | 43.4
| YRI | 0.0 | 9.5 | 90.5
| ASW | 0.0 | 17.5 | 82.5
| CHB | 19.7 | 47.4 | 32.8
| CHD | 21.1 | 45.0 | 33.9
| GIH | 1.0 | 23.8 | 75.2
| LWK | 0.0 | 21.8 | 78.2
| MEX | 12.3 | 40.4 | 47.4
| MKK | 2.6 | 25.0 | 72.4
| TSI | 2.0 | 35.3 | 62.7
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs9315385
|PubMedID=17903306
|Condition=Heart rate variability traits
|Gene=DCAMKL1
|Risk Allele=
|pValue=8.00E-006
|OR=NA
|95CI=
|OA=1
}}

{{PharmGKB
|RSID=rs9315385
|Name_s=
|Gene_s=DCLK1
|Feature=
|Evidence=PubMed ID:17903306; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study (Initial Sample Size: 548-1,175 individuals, depending on measure (Framingham); Replication Sample Size: NR). This variant is associated with Heart rate variability traits.
|Drugs=
|Drug Classes=
|Diseases=Cardiovascular Diseases
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356511
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9315385
|overall_frequency_n=17
|overall_frequency_d=126
|overall_frequency=0.134921
|n_genomes=12
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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