{{Rsnum
|rsid=121909241
|Chromosome=10
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PTEN
|position=87933154
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTEN
}}{{omim
|id=601728
|rsnum=121909241
|variant=0041
}}{{ClinVar
|rsid=121909241
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=89692911
|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; 2
|CLNHGVS=NC_000010.10:g.89692911G>A; NC_000010.10:g.89692911G>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=8741; 601728.0041
|CLNSIG=5
|CLNCUI=C1959582
|CLNDBN=not provided; PTEN hamartoma tumor syndrome
|Disease=not provided; PTEN hamartoma tumor syndrome
|CLNACC=RCV000078616.1; RCV000008302.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1488:C1959582
}}