{{Rsnum
|rsid=1059060
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PMS2
|position=5977709
|Status=Merged
|Merged=17420802
|Gene_s=PMS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.8 | 55.4 | 10.8
| HCB | 11.9 | 35.7 | 52.4
| JPT | 0.0 | 32.6 | 67.4
| YRI | 27.0 | 63.5 | 9.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.9 | 35.7 | 52.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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|17267408|OA=1
}} Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.{{GET Evidence
|gene=PMS2
|aa_change=Asn775Ser
|aa_change_short=N775S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1059060
|overall_frequency_n=2
|overall_frequency_d=126
|overall_frequency=0.015873
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.999
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=4
|webscore=N
}}