{{Rsnum
|rsid=10493340
|Chromosome=1
|position=63125458
|Orientation=plus
|GMAF=0.1947
|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 | 64.6 | 32.3 | 3.1
| HCB | 95.6 | 4.4 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 54.0 | 42.9 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 95.6 | 4.4 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs10493340
|PubMedID=17903302
|Condition=Blood pressure
|Gene=Intergenic
|Risk Allele=
|pValue=2.00E-006
|OR=NA
|95CI=
|OA=1
}}
{{PMID|17903302|OA=1
}} systolic blood pressure

{{PharmGKB
|RSID=rs10493340
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:17903302; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness (Initial Sample Size: 644-1,327 individuals, depending on measure (Framingham); Replication Sample Size: NR). This variant is associated with Blood pressure.
|Drugs=
|Drug Classes=
|Diseases=Cardiovascular Diseases
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356423
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10493340
|overall_frequency_n=31
|overall_frequency_d=128
|overall_frequency=0.242188
|n_genomes=25
|n_genomes_annotated=0
|n_haplomes=30
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}