{{Rsnum
|rsid=3118905
|Chromosome=13
|position=50531198
|Orientation=plus
|GMAF=0.1556
|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 | 3.2 | 41.3 | 55.6
| HCB | 0.0 | 2.3 | 97.7
| JPT | 0.0 | 4.4 | 95.6
| YRI | 0.0 | 19.0 | 81.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 2.3 | 97.7
| 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
}}{{PMID Auto GWAS
  |PMID=20881960
  |Trait=Height
  |Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height.
  |RiskAllele=A
  |Pval=1E-45
  |OR=.06
  |ORtxt=[NR] unit decrease
  |OA=1
}}

{{PMID Auto
|PMID=19570815
|Title=A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
|OA=1
}}

{{on chip | FTDNA}}