{{Rsnum
|rsid=121909226
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTEN
|position=87925557
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTEN
}}{{omim
|id=601728
|rsnum=121909226
|variant=0012
}}{{ClinVar
|rsid=121909226
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=89685314
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PTEN:5728
|GENE_NAME=PTEN
|GENE_ID=5728
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.89685314T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601728.0012
|CLNSIG=5
|CLNCUI=C2676500
|CLNDBN=Cowden syndrome
|Disease=Cowden syndrome
|CLNACC=RCV000008272.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1488:C0018553:158350:58037000
}}