{{Rsnum
|rsid=207906
|Gene=XRCC5
|Chromosome=2
|position=216148178
|Orientation=plus
|GMAF=0.1065
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=XRCC5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 25.0 | 74.1
| HCB | 1.5 | 16.1 | 82.5
| JPT | 0.0 | 21.2 | 78.8
| YRI | 4.1 | 23.1 | 72.8
| ASW | 0.0 | 19.3 | 80.7
| CHB | 1.5 | 16.1 | 82.5
| CHD | 2.8 | 15.6 | 81.7
| GIH | 7.9 | 25.7 | 66.3
| LWK | 0.9 | 20.9 | 78.2
| MEX | 1.7 | 19.0 | 79.3
| MKK | 0.0 | 21.2 | 78.8
| TSI | 1.0 | 26.5 | 72.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=21346221
|Title=Risk of acute promyelocytic leukemia in multiple sclerosis: Coding variants of DNA repair genes
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}