{{Rsnum
|rsid=63751207
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MSH2
|position=47466718
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSH2
}}{{omim
|id=609309
|rsnum=63751207
|variant=0007
}}

{{ClinVar
|rsid=63751207
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=47693857
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MSH2:4436
|GENE_NAME=MSH2
|GENE_ID=4436
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000002.11:g.47693857G>C; NC_000002.11:g.47693857G>T
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.1571G>C; 609309.0007; c.1571G>T
|CLNSIG=5
|CLNCUI=C2936783
|CLNDBN=Lynch syndrome I; Lynch syndrome
|Disease=Lynch syndrome I; Lynch syndrome
|CLNACC=RCV000001829.1; RCV000076197.1; RCV000076198.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C2936783:120435:144; NBK1211:C0009405:315058005
}}

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