{{Rsnum
|rsid=1802127
|Gene=MSH5
|Chromosome=6
|position=31762148
|Orientation=plus
|GMAF=0.04959
|Gene_s=C6orf26,MSH5
|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 | 97.3 | 2.7 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 66.7 | 31.3 | 2.0
| ASW | 75.0 | 25.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 82.7 | 15.5 | 1.8
| MEX | 81.0 | 17.2 | 1.7
| MKK | 75.6 | 23.7 | 0.6
| TSI | 93.1 | 6.9 | 0.0
| HapMapRevision=28
}}

{{ population diversity
| geno1 = (C;C)
| geno2 = (C;T)
| geno3 = (T;T)
| CEU | 98.3 | 1.7 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 70.0 | 26.7 | 3.3
}}

{{PMID Auto
|PMID=16741161
|Title=Variants in the GH-IGF axis confer susceptibility to lung cancer.
|OA=1
}}

{{PMID Auto
|PMID=17409188
|Title=Role for Msh5 in the regulation of Ig class switch recombination.
|OA=1
}}

{{GET Evidence
|gene=MSH5
|aa_change=Pro787Ser
|aa_change_short=P787S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1802127
|overall_frequency_n=599
|overall_frequency_d=10758
|overall_frequency=0.0556795
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23238918
|Title=Genome-wide pathway analysis of a genome-wide association study on multiple sclerosis.
}}

{{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}}