{{Rsnum
|rsid=63750393
|Chromosome=2
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GA)
|geno3=(GA;GA)
|Gene=MSH2
|position=47471008
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=63750393
|Reversed=0
|FwdREF=GA
|FwdALT=
|REF=AGA
|ALT=A
|RSPOS=47698146
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100200
|GENEINFO=MSH2:4436
|GENE_NAME=MSH2
|GENE_ID=4436
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47698147_47698148delGA
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Lynch syndrome
|Disease=Lynch syndrome
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030243.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNSRCID=c.1705_1706del
}}{{PMID Auto
|PMID=20007
|Title=[A case of acute ischemia of the extremities in disseminated intravascular coagulation in an infant].
}}

{{PMID Auto
|PMID=11920650
|Title=Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain.
}}

{{PMID Auto
|PMID=12362047
|Title=Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States.
|OA=1
}}

{{PMID Auto
|PMID=12414824
|Title=Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation.
|OA=1
}}

{{PMID Auto
|PMID=19698169
|Title=Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario.
|OA=1
}}

{{PMID Auto
|PMID=19706203
|Title=Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.
|OA=1
}}