{{Rsnum
|rsid=267608153
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PMS2
|position=5995534
|Gene_s=PMS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000076896.1
|CLNALLE=1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000007.13:g.6035165C>A
|CLNSIG=4
|CLNSRC=InSiGHT
|CLNSRCID=c.903G>T
|Disease=Lynch syndrome
|FwdALT=T
|FwdREF=G
|GENEINFO=PMS2:5395
|GENE_ID=5395
|GENE_NAME=PMS2
|REF=C
|RSPOS=6035165
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050260000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=267608153
}}