{{Rsnum
|rsid=749052
|Chromosome=2
|position=231931900
|Orientation=minus
|GMAF=0.05923
|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 | 85.0 | 14.2 | 0.9
| HCB | 97.8 | 2.2 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 71.4 | 27.9 | 0.7
| ASW | 80.7 | 17.5 | 1.8
| CHB | 97.8 | 2.2 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 88.0 | 12.0 | 0.0
| LWK | 85.3 | 14.7 | 0.0
| MEX | 98.3 | 1.7 | 0.0
| MKK | 86.4 | 13.6 | 0.0
| TSI | 77.5 | 20.6 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18391951
|Trait=Height
|Title=Many sequence variants affecting diversity of adult human height
|RiskAllele=A
|Pval=9.9999999999999995E-7
|OR=8.70
|ORtxt=[5.17-12.23] % SD taller
}}

{{PMID|18471798|OA=1
}} Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.

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

{{PMID|20017971|OA=1
}} Assessing the impact of global versus local ancestry in association studies.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs749052
|overall_frequency_n=10
|overall_frequency_d=128
|overall_frequency=0.078125
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=9
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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