{{Rsnum
|rsid=10800485
|Gene=SCYL3
|Chromosome=1
|position=169878005
|Orientation=plus
|GMAF=0.331
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SCYL3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 41.6 | 48.7
| HCB | 27.0 | 55.5 | 17.5
| JPT | 35.4 | 54.0 | 10.6
| YRI | 1.4 | 15.1 | 83.6
| ASW | 3.6 | 16.1 | 80.4
| CHB | 27.0 | 55.5 | 17.5
| CHD | 25.7 | 52.3 | 22.0
| GIH | 5.9 | 36.6 | 57.4
| LWK | 0.9 | 25.5 | 73.6
| MEX | 5.2 | 46.6 | 48.3
| MKK | 1.3 | 18.6 | 80.1
| TSI | 4.9 | 45.1 | 50.0
| HapMapRevision=28
}}

{{PMID Auto
|PMID=17357082
|Title=Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
|OA=1
}}

{{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}}
{{on chip | NatGeo2}}