{{Rsnum
|rsid=9536591
|Chromosome=13
|position=54006952
|Orientation=plus
|GMAF=0.4972
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 31.0 | 44.2 | 24.8
| HCB | 12.6 | 44.4 | 43.0
| JPT | 16.1 | 44.6 | 39.3
| YRI | 36.1 | 42.9 | 21.1
| ASW | 31.6 | 45.6 | 22.8
| CHB | 12.6 | 44.4 | 43.0
| CHD | 14.7 | 45.9 | 39.4
| GIH | 17.8 | 44.6 | 37.6
| LWK | 23.6 | 54.5 | 21.8
| MEX | 44.8 | 43.1 | 12.1
| MKK | 24.4 | 52.6 | 23.1
| TSI | 24.5 | 56.9 | 18.6
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs9536591
|PubMedID=17434096
|Condition=Stroke
|Gene=Intergenic
|Risk Allele=
|pValue=6.00E-006
|OR=1.92
|95CI=1.41-2.63
|OA=1
}}

{{PharmGKB
|RSID=rs9536591
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:17434096; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release (Initial Sample Size: 259 cases, 269 controls; Replication Sample Size: NR). This variant is associated with Stroke.
|Drugs=
|Drug Classes=
|Diseases=Stroke
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356394
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9536591
|overall_frequency_n=52
|overall_frequency_d=128
|overall_frequency=0.40625
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=44
|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 | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}