{{Rsnum
|rsid=2303426
|Gene=MSH2
|Chromosome=2
|position=47403411
|Orientation=plus
|GMAF=0.3843
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=MSH2
}}{{PMID Auto
|PMID=21283657
|Title=Gallbladder Cancer Predisposition: A Multigenic Approach to DNA-Repair, Apoptotic and Inflammatory Pathway Genes
|OA=1
}}{{ClinVar
|rsid=2303426
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=47630550
|CHROM=2
|GMAF=0.3846
|dbSNPBuildID=100
|SSR=0
|SAO=1
|VP=0x05016800000017011e100100
|GENEINFO=MSH2:4436
|GENE_NAME=MSH2
|GENE_ID=4436
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47630550C>G
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=2
|CLNDBN=Lynch syndrome; AllHighlyPenetrant
|Disease=Lynch syndrome; AllHighlyPenetrant
|Tags=PM;PMC;SLO;VLD;G5A;G5;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD
|CAF=0.3843; 0.6157
|CLNACC=RCV000030249.2; RCV000035360.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1211:C0009405:315058005; CN169374
|COMMON=1
|CLNSRCID=c.211+9C>G
}}{{PMID Auto
|PMID=20564624
|Title=Polymorphisms in ERCC2, MSH2, and OGG1 DNA repair genes and gallbladder cancer risk in a population of Northern India.
}}