{{Rsnum
|rsid=2075789
|Gene=MSH5
|Chromosome=6
|position=31740551
|Orientation=minus
|GMAF=0.1212
|Gene_s=MSH5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 21.4 | 78.6
| HCB | 2.2 | 27.6 | 70.1
| JPT | 8.9 | 36.6 | 54.5
| YRI | 0.0 | 2.0 | 98.0
| ASW | 0.0 | 19.3 | 80.7
| CHB | 2.2 | 27.6 | 70.1
| CHD | 4.7 | 18.7 | 76.6
| GIH | 2.0 | 24.0 | 74.0
| LWK | 0.0 | 3.7 | 96.3
| MEX | 1.8 | 22.8 | 75.4
| MKK | 3.3 | 14.0 | 82.7
| TSI | 1.0 | 18.6 | 80.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=22594646
|Title=Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility
|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=Pro29Ser
|aa_change_short=P29S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2075789
|overall_frequency_n=610
|overall_frequency_d=9782
|overall_frequency=0.0623594
|n_genomes=4
|n_genomes_annotated=0
|n_haplomes=4
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

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