{{Rsnum
|rsid=7187365
|Gene=FENDRR
|Chromosome=16
|position=86478309
|Orientation=plus
|GMAF=0.1901
|Gene_s=FENDRR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 76.1 | 22.1 | 1.8
| HCB | 53.3 | 40.9 | 5.8
| JPT | 71.7 | 24.8 | 3.5
| YRI | 68.7 | 28.6 | 2.7
| ASW | 52.6 | 40.4 | 7.0
| CHB | 53.3 | 40.9 | 5.8
| CHD | 50.5 | 42.2 | 7.3
| GIH | 54.5 | 34.7 | 10.9
| LWK | 65.5 | 31.8 | 2.7
| MEX | 77.6 | 19.0 | 3.4
| MKK | 68.6 | 27.6 | 3.8
| TSI | 60.8 | 36.3 | 2.9
| 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=C
  |Pval=6E-6
  |OR=1.22
  |ORtxt=[1.12-1.33]
  }}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}