{{Rsnum
|rsid=1048466
|Gene=CCDC77
|Chromosome=12
|position=442384
|Orientation=plus
|GMAF=0.242
|Gene_s=CCDC77
|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 | 3.5 | 42.5 | 54.0
| HCB | 6.6 | 37.2 | 56.2
| JPT | 19.5 | 41.6 | 38.9
| YRI | 3.4 | 26.5 | 70.1
| ASW | 0.0 | 43.9 | 56.1
| CHB | 6.6 | 37.2 | 56.2
| CHD | 12.0 | 35.2 | 52.8
| GIH | 2.0 | 30.7 | 67.3
| LWK | 1.8 | 30.9 | 67.3
| MEX | 3.4 | 22.4 | 74.1
| MKK | 1.3 | 23.1 | 75.6
| TSI | 3.9 | 26.5 | 69.6
| 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=G
  |Pval=8E-8
  |OR=1.22
  |ORtxt=[1.14-1.32]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}