{{Rsnum
|rsid=1963982
|Gene=LOC392232
|Chromosome=8
|position=72194681
|Orientation=minus
|GMAF=0.4077
|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 | 19.6 | 50.0 | 30.4
| HCB | 13.1 | 55.5 | 31.4
| JPT | 23.0 | 48.7 | 28.3
| YRI | 8.2 | 41.8 | 50.0
| ASW | 8.8 | 42.1 | 49.1
| CHB | 13.1 | 55.5 | 31.4
| CHD | 14.0 | 49.5 | 36.4
| GIH | 21.0 | 48.0 | 31.0
| LWK | 13.6 | 34.5 | 51.8
| MEX | 15.5 | 58.6 | 25.9
| MKK | 9.7 | 39.6 | 50.6
| TSI | 18.8 | 48.5 | 32.7
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs1963982
|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=rs1963982
|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=PA162356424
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1963982
|overall_frequency_n=52
|overall_frequency_d=128
|overall_frequency=0.40625
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=46
|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 | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}