{{Rsnum
|rsid=193922373
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MSH2
|position=47408493
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922373
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=47635632
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47635632G>A
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=3
|CLNDBN=Lynch syndrome
|Disease=Lynch syndrome
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030251.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|CLNSRCID=c.304G>A_2
}}{{PMID Auto
|PMID=12200596
|Title=Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer.
}}

{{PMID Auto
|PMID=17192056
|Title=The use of microsatellite instability, immunohistochemistry and other variables in determining the clinical significance of MLH1 and MSH2 unclassified variants in Lynch syndrome.
}}

{{PMID Auto
|PMID=18383312
|Title=Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).
}}