{{Rsnum
|rsid=121434629
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PMS2
|position=6005918
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMS2
}}{{omim
|id=600259
|rsnum=121434629
|variant=0012
}}{{ClinVar
|rsid=121434629
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=6045549
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PMS2:5395
|GENE_NAME=PMS2
|GENE_ID=5395
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.6045549C>A; NC_000007.13:g.6045549C>T
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.137G>T_2; 600259.0012; c.137G>A
|CLNSIG=5
|CLNCUI=C0265325
|CLNDBN=Turcot syndrome; Hereditary nonpolyposis colorectal cancer type 4; Lynch syndrome
|Disease=Turcot syndrome; Hereditary nonpolyposis colorectal cancer type 4; Lynch syndrome
|CLNACC=RCV000009826.2; RCV000056324.1; RCV000076807.1; RCV000076806.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0265325:276300:252202:61665008; C1838333:614337:144; NBK1211:C0009405:315058005
}}