{{Rsnum
|rsid=2019877
|Gene=C17orf54
|Chromosome=17
|position=73763821
|Orientation=plus
|GMAF=0.3829
|Gene_s=LINC00469
|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 | 25.2 | 55.0 | 19.8
| HCB | 25.9 | 52.6 | 21.5
| JPT | 29.2 | 46.9 | 23.9
| YRI | 78.9 | 21.1 | 0.0
| ASW | 61.4 | 31.6 | 7.0
| CHB | 25.9 | 52.6 | 21.5
| CHD | 39.4 | 54.1 | 6.4
| GIH | 27.3 | 43.4 | 29.3
| LWK | 80.0 | 19.1 | 0.9
| MEX | 30.4 | 57.1 | 12.5
| MKK | 64.3 | 28.6 | 7.1
| TSI | 31.7 | 49.5 | 18.8
| HapMapRevision=28
}}

{{omim
|desc=PONTOCEREBELLAR HYPOPLASIA TYPE 2A; PCH2A
|id=277470
|rsnum=2019877
}}

{{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}}