{{Rsnum
|rsid=1741344
|Chromosome=20
|position=4121153
|Orientation=plus
|GMAF=0.3053
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC101929155
|Gene_s=LOC101929155
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 13.3 | 46.0 | 40.7
| HCB | 4.4 | 30.7 | 65.0
| JPT | 2.7 | 29.2 | 68.1
| YRI | 24.0 | 48.6 | 27.4
| ASW | 12.3 | 52.6 | 35.1
| CHB | 4.4 | 30.7 | 65.0
| CHD | 4.6 | 26.6 | 68.8
| GIH | 5.0 | 32.7 | 62.4
| LWK | 10.9 | 49.1 | 40.0
| MEX | 8.6 | 34.5 | 56.9
| MKK | 10.3 | 37.2 | 52.6
| TSI | 10.8 | 42.2 | 47.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20881960
|Trait=None
|Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height.
|RiskAllele=T
|Pval=3E-9
|OR=0.0200
|ORtxt=[NR] meters decrease
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}