{{Rsnum
|rsid=2275848
|Gene=NINJ1
|Chromosome=9
|position=93125038
|Orientation=plus
|GMAF=0.2048
|Gene_s=NINJ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 4.4 | 22.1 | 73.5
| HCB | 0.7 | 17.6 | 81.6
| JPT | 5.3 | 30.1 | 64.6
| YRI | 10.9 | 48.3 | 40.8
| ASW | 15.8 | 33.3 | 50.9
| CHB | 0.7 | 17.6 | 81.6
| CHD | 0.9 | 17.4 | 81.7
| GIH | 2.0 | 28.7 | 69.3
| LWK | 17.3 | 39.1 | 43.6
| MEX | 0.0 | 15.5 | 84.5
| MKK | 3.2 | 45.5 | 51.3
| TSI | 7.8 | 40.2 | 52.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23563609
  |Trait=Obesity (early onset extreme)
  |Title=Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
  |RiskAllele=T
  |Pval=1E-6
  |OR=1.23
  |ORtxt=[1.13-1.34]
  }}

{{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 | Illumina Human 1M}}