{{Rsnum
|rsid=63750871
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PMS2
|position=6002590
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMS2
}}{{omim
|id=600259
|rsnum=63750871
|variant=0001
}}

{{ClinVar
|rsid=63750871
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=6042221
|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.6042221G>A
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.400C>T; 600259.0001
|CLNSIG=5
|CLNCUI=C0265325
|CLNDBN=Turcot syndrome; Lynch syndrome
|Disease=Turcot syndrome; Lynch syndrome
|CLNACC=RCV000009815.3; RCV000076872.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0265325:276300:252202:61665008; NBK1211:C0009405:315058005
}}

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