{{Rsnum
|rsid=935334
|Chromosome=14
|position=76147335
|Orientation=plus
|GMAF=0.208
|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 | 76.6 | 22.5 | 0.9
| HCB | 76.5 | 21.3 | 2.2
| JPT | 68.1 | 26.5 | 5.3
| YRI | 34.9 | 51.4 | 13.7
| ASW | 42.1 | 45.6 | 12.3
| CHB | 76.5 | 21.3 | 2.2
| CHD | 65.7 | 30.6 | 3.7
| GIH | 88.1 | 10.9 | 1.0
| LWK | 29.1 | 58.2 | 12.7
| MEX | 67.2 | 29.3 | 3.4
| MKK | 26.3 | 50.6 | 23.1
| TSI | 68.6 | 30.4 | 1.0
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs935334
|PubMedID=17903302
|Condition=Blood pressure
|Gene=Intergenic
|Risk Allele=
|pValue=3.00E-006
|OR=NA
|95CI=
|OA=1
}}
{{PMID|17903302|OA=1
}} diastolic blood pressure

{{PharmGKB
|RSID=rs935334
|Name_s=
|Gene_s=C14orf118
|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=PA162356425
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs935334
|overall_frequency_n=90
|overall_frequency_d=128
|overall_frequency=0.703125
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=76
|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}}