{{Rsnum
|rsid=121909224
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTEN
|position=87933147
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTEN
}}{{omim
|id=601728
|rsnum=121909224
|variant=0007
}}{{ClinVar
|rsid=121909224
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=89692904
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050260000000000002110120
|GENEINFO=PTEN:5728
|GENE_NAME=PTEN
|GENE_ID=5728
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000010.10:g.89692904C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=3128; 601728.0007
|CLNCUI=.,C0018553; C0265326; C1854416
|CLNDBN=Cowden syndrome; Bannayan-Riley-Ruvalcaba syndrome; Macrocephaly/autism syndrome; not provided
|Disease=Cowden syndrome; Bannayan-Riley-Ruvalcaba syndrome; Macrocephaly/autism syndrome; not provided
|CLNACC=RCV000008263.2; RCV000008264.1; RCV000008265.1; RCV000078615.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1488:C0018553:158350:58037000; NBK1488:C0265326:153480:109; C1854416:605309:210548
|CLNSIG=5
}}