{{Rsnum
|rsid=2326458
|Chromosome=16
|position=84954073
|Orientation=plus
|GMAF=0.3255
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 69.0 | 28.3 | 2.7
| HCB | 45.3 | 41.6 | 13.1
| JPT | 45.1 | 46.0 | 8.8
| YRI | 27.2 | 49.0 | 23.8
| ASW | 45.6 | 33.3 | 21.1
| CHB | 45.3 | 41.6 | 13.1
| CHD | 40.4 | 56.9 | 2.8
| GIH | 34.7 | 55.4 | 9.9
| LWK | 28.2 | 40.9 | 30.9
| MEX | 33.3 | 50.9 | 15.8
| MKK | 22.4 | 54.5 | 23.1
| TSI | 57.8 | 35.3 | 6.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=18391951
|Trait=Height
|Title=Many sequence variants affecting diversity of adult human height
|RiskAllele=C
|Pval=7.9999999999999996E-7
|OR=5.10
|ORtxt=[3.14-7.06] % SD taller
}}

{{omim
|id=613547
|rsnum=2326458
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2326458
|overall_frequency_n=86
|overall_frequency_d=128
|overall_frequency=0.671875
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=76
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}