{{Rsnum
|rsid=8099594
|Chromosome=18
|position=49464790
|Orientation=plus
|GMAF=0.4665
|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 | 35.4 | 49.6 | 15.0
| HCB | 20.0 | 37.0 | 43.0
| JPT | 10.6 | 47.8 | 41.6
| YRI | 29.9 | 42.2 | 27.9
| ASW | 19.3 | 56.1 | 24.6
| CHB | 20.0 | 37.0 | 43.0
| CHD | 16.8 | 49.5 | 33.6
| GIH | 31.0 | 49.0 | 20.0
| LWK | 17.3 | 48.2 | 34.5
| MEX | 39.7 | 48.3 | 12.1
| MKK | 34.8 | 43.9 | 21.3
| TSI | 47.1 | 40.2 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18391952
|Trait=Height
|Title=Genome-wide association analysis identifies 20 loci that influence adult height
|RiskAllele=A
|Pval=2.9999999999999999E-7
|OR=0.05
|ORtxt= [0.02-0.08] SD taller - among males
|OA=1
}}

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

{{PMID Auto
|PMID=20846217
|Title=Association of linear growth impairment in pediatric Crohn's disease and a known height locus: a pilot study.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8099594
|overall_frequency_n=68
|overall_frequency_d=128
|overall_frequency=0.53125
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=56
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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