{{Rsnum
|rsid=6724465
|Gene=NHEJ1
|Chromosome=2
|position=219079124
|Orientation=plus
|GMAF=0.1111
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NHEJ1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 19.5 | 79.6
| HCB | 2.9 | 23.4 | 73.7
| JPT | 1.8 | 35.7 | 62.5
| YRI | 2.1 | 30.1 | 67.8
| ASW | 1.8 | 24.6 | 73.7
| CHB | 2.9 | 23.4 | 73.7
| CHD | 0.0 | 19.3 | 80.7
| GIH | 0.0 | 7.9 | 92.1
| LWK | 0.9 | 12.8 | 86.2
| MEX | 0.0 | 24.1 | 75.9
| MKK | 3.8 | 29.5 | 66.7
| TSI | 1.0 | 13.7 | 85.3
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=18391952
|Trait=Height
|Title=Genome-wide association analysis identifies 20 loci that influence adult height
|RiskAllele=A
|Pval=2E-8
|OR=0.06
|ORtxt=[0.02-0.10] SD shorter - among males
|OA=1
}}

{{PMID Auto
|PMID=19030899
|Title=Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
|OA=1
}}

{{PMID Auto
|PMID=19039035
|Title=Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
|OA=1
}}

{{PMID Auto
|PMID=19481195
|Title=The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
|OA=1
}}

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6724465
|overall_frequency_n=15
|overall_frequency_d=128
|overall_frequency=0.117188
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=13
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
|n_web_uneval=10
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}