{{Rsnum
|rsid=2619566
|Gene=CNTN4
|Chromosome=3
|position=2583254
|Orientation=minus
|GMAF=0.3416
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CNTN4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 15.0 | 83.2
| HCB | 19.0 | 54.0 | 27.0
| JPT | 24.8 | 52.2 | 23.0
| YRI | 33.3 | 48.3 | 18.4
| ASW | 26.3 | 36.8 | 36.8
| CHB | 19.0 | 54.0 | 27.0
| CHD | 16.5 | 48.6 | 34.9
| GIH | 17.8 | 48.5 | 33.7
| LWK | 33.6 | 50.9 | 15.5
| MEX | 5.2 | 50.0 | 44.8
| MKK | 14.7 | 52.6 | 32.7
| TSI | 2.9 | 13.7 | 83.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19451621
|Trait=Amyotrophic lateral sclerosis
|Title=Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis
|RiskAllele=G
|Pval=0.000007
|OR=3.03
|ORtxt=[1.71-4.35] years younger
|OA=1
}}

{{PMID Auto
|PMID=17903301
|Title=Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2619566
|overall_frequency_n=82
|overall_frequency_d=128
|overall_frequency=0.640625
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=72
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}