{{Rsnum
|rsid=7591163
|Chromosome=2
|position=227850659
|Orientation=plus
|GMAF=0.3554
|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 | 5.3 | 36.3 | 58.4
| HCB | 31.4 | 55.5 | 13.1
| JPT | 25.7 | 43.4 | 31.0
| YRI | 17.0 | 48.3 | 34.7
| ASW | 14.0 | 43.9 | 42.1
| CHB | 31.4 | 55.5 | 13.1
| CHD | 34.9 | 46.8 | 18.3
| GIH | 5.9 | 38.6 | 55.4
| LWK | 20.0 | 50.9 | 29.1
| MEX | 5.2 | 32.8 | 62.1
| MKK | 16.0 | 46.8 | 37.2
| TSI | 2.0 | 38.2 | 59.8
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=17903302
|Trait=Blood pressure
|Title=Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
|RiskAllele=
|Pval=2.9999999999999999E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7591163
|overall_frequency_n=93
|overall_frequency_d=128
|overall_frequency=0.726562
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=77
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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