{{Rsnum
|rsid=7129220
|Chromosome=11
|position=10328991
|Orientation=plus
|GMAF=0.073
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CAND1.11
|Gene_s=CAND1.11
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 19.5 | 79.6
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.7 | 9.5 | 89.8
| ASW | 0.0 | 7.0 | 93.0
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 6.9 | 93.1
| LWK | 0.9 | 13.0 | 86.1
| MEX | 0.0 | 8.6 | 91.4
| MKK | 2.6 | 28.4 | 69.0
| TSI | 0.0 | 20.6 | 79.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=G
|Pval=6E-8
|OR=0.2990
|ORtxt=[NR] mmHg decrease
|OA=1
}}
{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=G
|Pval=4E-7
|OR=0.3800
|ORtxt=[0.23-0.53] mmHg decrease
|OA=1
}}

{{PMID Auto
|PMID=19039035
|Title=Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}