{{Rsnum
|rsid=1053839
|Gene=C20orf79
|Chromosome=20
|position=18814110
|Orientation=plus
|GMAF=0.2006
|Gene_s=C20orf79,LOC100128496
|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 | 69.9 | 25.7 | 4.4
| HCB | 91.0 | 9.0 | 0.0
| JPT | 80.9 | 18.2 | 0.9
| YRI | 35.9 | 46.2 | 17.9
| ASW | 36.8 | 49.1 | 14.0
| CHB | 91.0 | 9.0 | 0.0
| CHD | 97.2 | 2.8 | 0.0
| GIH | 68.0 | 29.0 | 3.0
| LWK | 35.8 | 44.0 | 20.2
| MEX | 66.1 | 28.6 | 5.4
| MKK | 54.5 | 39.6 | 5.8
| TSI | 66.3 | 28.7 | 5.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19574904
|Title=Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval
|OA=1
}}

{{GET Evidence
|gene=C20ORF79
|aa_change=Pro99Ser
|aa_change_short=P99S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1053839
|overall_frequency_n=2622
|overall_frequency_d=10758
|overall_frequency=0.243726
|n_genomes=27
|n_genomes_annotated=0
|n_haplomes=32
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}