{{Rsnum
|rsid=121434630
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=PMS2
|position=6004003
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMS2
}}{{omim
|id=600259
|rsnum=121434630
|variant=0016
}}{{ClinVar
|rsid=121434630
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=6043634
|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
|CLNHGVS=NC_000007.13:g.6043634A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600259.0016
|CLNSIG=5
|CLNCUI=C0265325
|CLNDBN=Turcot syndrome
|Disease=Turcot syndrome
|CLNACC=RCV000009830.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1211:C0265325:276300:252202:61665008
}}