{{Rsnum
|rsid=63751449
|Chromosome=2
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=MSH2
|position=47410181
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000001839.1; RCV000076602.1
|CLNALLE=1
|CLNDBN=Turcot syndrome; Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0265325:276300:252202:61665008; NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47637320delA
|CLNSIG=5
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNSRCID=c.454del; 609309.0016
|Disease=Turcot syndrome; Lynch syndrome
|FwdREF=A
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=TA
|RSPOS=47637316
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=DIV
|VP=0x050260000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=63751449
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}