{{Rsnum
|rsid=4258342
|Gene=CNTN5
|Chromosome=11
|position=99994516
|Orientation=plus
|GMAF=0.3255
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CNTN5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 50.0 | 40.0 | 10.0
| HCB | 78.2 | 20.3 | 1.5
| JPT | 80.6 | 15.7 | 3.7
| YRI | 8.3 | 46.5 | 45.1
| ASW | 21.1 | 35.1 | 43.9
| CHB | 78.2 | 20.3 | 1.5
| CHD | 76.9 | 21.3 | 1.9
| GIH | 37.5 | 50.0 | 12.5
| LWK | 0.0 | 0.0 | 0.0
| MEX | 60.7 | 32.1 | 7.1
| MKK | 19.6 | 52.0 | 28.4
| TSI | 45.0 | 40.0 | 15.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs4258342
|Name_s=
|Gene_s=CNTN5
|Feature=
|Evidence=PubMed ID:17537913
|Annotation=Risk or phenotype-associated allele: not stated Phenotype: Using a Quantitative Transmission Disequilibrium Test (QTDT), this variant was significantly associated with etoposide toxicity based upon IC50 values in cell lines from 30 parent-child trios. Study size: 89. Study population/ethnicity: 89 Yorubans. Significance metric(s): p = 0.00006. Type of association: FA; GN.
|Drugs=etoposide
|Drug Classes=
|Diseases=Drug Toxicity
|Curation Level=Curated
|PharmGKB Accession ID=PA165109359
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4258342
|overall_frequency_n=43
|overall_frequency_d=118
|overall_frequency=0.364407
|n_genomes=30
|n_genomes_annotated=0
|n_haplomes=37
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}