{{Rsnum
|rsid=63750451
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PMS2
|position=5986883
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMS2
}}{{omim
|id=600259
|rsnum=63750451
|variant=0009
}}

{{ClinVar
|rsid=63750451
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=6026514
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PMS2:5395
|GENE_NAME=PMS2
|GENE_ID=5395
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.6026514G>A
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.1882C>T; 600259.0009
|CLNSIG=5
|CLNCUI=C1838333
|CLNDBN=Hereditary nonpolyposis colorectal cancer type 4; Lynch syndrome
|Disease=Hereditary nonpolyposis colorectal cancer type 4; Lynch syndrome
|CLNACC=RCV000009823.3; RCV000076834.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=C1838333:614337:144; NBK1211:C0009405:315058005
}}

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