{{Rsnum
|rsid=1572931
|Gene=RAB7L1
|Chromosome=1
|position=205775090
|Orientation=plus
|GMAF=0.2149
|Gene_s=RAB7L1
|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 | 75.2 | 23.0 | 1.8
| HCB | 43.1 | 47.4 | 9.5
| JPT | 31.9 | 46.0 | 22.1
| YRI | 87.8 | 12.2 | 0.0
| ASW | 82.5 | 17.5 | 0.0
| CHB | 43.1 | 47.4 | 9.5
| CHD | 42.2 | 45.0 | 12.8
| GIH | 64.4 | 31.7 | 4.0
| LWK | 76.4 | 22.7 | 0.9
| MEX | 41.4 | 44.8 | 13.8
| MKK | 67.9 | 30.8 | 1.3
| TSI | 70.6 | 24.5 | 4.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=22232350
|Title=Association of Sequence Alterations in the Putative Promoter of RAB7L1 With a Reduced Parkinson Disease Risk
}}

{{PMID Auto
|PMID=25040112
|Title=An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China
}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}