{{Rsnum
|rsid=4327572
|Chromosome=5
|position=25972712
|Orientation=plus
|GMAF=0.2397
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 36.9 | 50.5 | 12.6
| HCB | 73.3 | 22.2 | 4.4
| JPT | 74.8 | 24.3 | 0.9
| YRI | 98.6 | 1.4 | 0.0
| ASW | 82.5 | 17.5 | 0.0
| CHB | 73.3 | 22.2 | 4.4
| CHD | 74.5 | 24.5 | 0.9
| GIH | 36.6 | 47.5 | 15.8
| LWK | 97.3 | 2.7 | 0.0
| MEX | 56.9 | 32.8 | 10.3
| MKK | 66.5 | 29.0 | 4.5
| TSI | 32.7 | 50.5 | 16.8
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs4327572
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19404256
|Annotation=This SNP on 5p14.1 was associated with autism spectrum disorder in a combined analysis of four GWAS data sets with a total of more than 10,000 subjects of European ancestry. This SNP is in an intergenic region between CDH10 and CDH9 that contains several highly conserved genomic elements.
|Drugs=
|Drug Classes=
|Diseases=Autism Spectrum Disorder
|Curation Level=Curated
|PharmGKB Accession ID=PA164741098
}}

{{PMID|19456320|OA=1
}} A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4327572
|overall_frequency_n=30
|overall_frequency_d=128
|overall_frequency=0.234375
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}