{{Rsnum
|rsid=1919128
|Gene=C2orf16
|Chromosome=2
|position=27578892
|Orientation=plus
|GMAF=0.3274
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=C2orf16
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 60.2 | 32.7 | 7.1
| HCB | 25.9 | 46.7 | 27.4
| JPT | 15.9 | 46.0 | 38.1
| YRI | 96.6 | 3.4 | 0.0
| ASW | 86.0 | 14.0 | 0.0
| CHB | 25.9 | 46.7 | 27.4
| CHD | 26.9 | 47.2 | 25.9
| GIH | 67.3 | 31.7 | 1.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 29.8 | 45.6 | 24.6
| MKK | 92.3 | 7.7 | 0.0
| TSI | 43.6 | 47.5 | 8.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21386085
|Trait=None
|Title=A Bivariate Genome-Wide Approach to Metabolic Syndrome: STAMPEED Consortium
|RiskAllele=A
|Pval=2E-9
|OR=0.1800
|ORtxt=[0.12-0.24] unit decrease
|OA=1
}}

{{GET Evidence
|gene=C2ORF16
|aa_change=Ile774Val
|aa_change_short=I774V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1919128
|overall_frequency_n=2002
|overall_frequency_d=9508
|overall_frequency=0.21056
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=30
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}