{{Rsnum
|rsid=397507541
|Chromosome=12
|position=112489068
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTPN11
|Gene_s=PTPN11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000033539.2; RCV000055885.1
|CLNALLE=1
|CLNDBN=Rasopathy; LEOPARD syndrome 1
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN166718; NBK1383:CN074218:151100:500
|CLNHGVS=NC_000012.11:g.112926872C>T
|CLNSIG=5
|Disease=Rasopathy; LEOPARD syndrome 1
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=112926872
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=397507541
|CLNSRC=GeneReviews
|CLNSRCID=NBK1383
|GENEINFO=PTPN11:5781
|GENE_ID=5781
|GENE_NAME=PTPN11
}}