{{Rsnum
|rsid=10486776
|Gene=RPL36AP26
|Chromosome=7
|position=15703161
|Orientation=plus
|GMAF=0.07576
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 10.8 | 89.2
| HCB | 3.1 | 26.7 | 70.2
| JPT | 0.0 | 14.0 | 86.0
| YRI | 0.0 | 4.3 | 95.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 3.1 | 26.7 | 70.2
| CHD | 1.9 | 29.0 | 69.2
| GIH | 5.0 | 13.9 | 81.2
| LWK | 0.0 | 4.7 | 95.3
| MEX | 1.8 | 8.8 | 89.5
| MKK | 0.6 | 5.8 | 93.6
| TSI | 4.0 | 29.7 | 66.3
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs10486776
|PubMedID=17434096
|Condition=Stroke
|Gene=Intergenic
|Risk Allele=
|pValue=6.00E-006
|OR=5.62
|95CI=2.66-11.9
|OA=1
}}

{{PharmGKB
|RSID=rs10486776
|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=PA162356393
}}

{{PMID|19910543}} Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10486776
|overall_frequency_n=6
|overall_frequency_d=128
|overall_frequency=0.046875
|n_genomes=6
|n_genomes_annotated=0
|n_haplomes=6
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
|n_web_uneval=10
}}

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