{{Rsnum
|rsid=121918468
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PTPN11
|position=112488444
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918468
|variant=0020
}}{{ClinVar
|rsid=121918468
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=112926248
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PTPN11:5781
|GENE_NAME=PTPN11
|GENE_ID=5781
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000012.11:g.112926248G>A; NC_000012.11:g.112926248G>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1383; 176876.0020
|CLNSIG=5
|CLNCUI=C0175704
|CLNDBN=LEOPARD syndrome; Rasopathy; Noonan's syndrome; LEOPARD syndrome 1
|Disease=LEOPARD syndrome; Rasopathy; Noonan's syndrome; LEOPARD syndrome 1
|CLNACC=RCV000014270.16; RCV000033530.2; RCV000037611.1; RCV000055882.1; RCV000033529.2; RCV000037612.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen; MedGen; GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1383:C0175704; CN166718; NBK1124:C0028326:163950:205824006; NBK1383:CN074218:151100:500
}}