{{Rsnum
|rsid=1062708
|Gene=RUVBL2
|Chromosome=19
|position=49010016
|Orientation=plus
|GMAF=0.427
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MIR6798,RUVBL2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 22.1 | 45.1 | 32.7
| HCB | 27.2 | 50.7 | 22.1
| JPT | 30.1 | 53.1 | 16.8
| YRI | 60.5 | 36.7 | 2.7
| ASW | 66.7 | 22.8 | 10.5
| CHB | 27.2 | 50.7 | 22.1
| CHD | 31.2 | 50.5 | 18.3
| GIH | 20.0 | 51.0 | 29.0
| LWK | 71.8 | 26.4 | 1.8
| MEX | 17.2 | 44.8 | 37.9
| MKK | 66.5 | 29.7 | 3.9
| TSI | 19.6 | 58.8 | 21.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=19403135
|Title=Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
}}

{{PMID|16251468|OA=1
}} Survey of allelic expression using EST mining.

{{PMID|19052777|OA=1
}} Identification of common genetic variants that account for transcript isoform variation between human populations.

{{PMID|19374514|OA=1
}} Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}