{{Rsnum
|rsid=121918470
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PTPN11
|position=112489105
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918470
|variant=0022
}}{{ClinVar
|rsid=121918470
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=112926909
|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.112926909A>C; NC_000012.11:g.112926909A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176876.0022; 176876.0023
|CLNSIG=5
|CLNCUI=C0175704; C0041409
|CLNDBN=LEOPARD syndrome; Rasopathy; Noonan syndrome 1
|Disease=LEOPARD syndrome; Rasopathy; Noonan syndrome 1
|CLNACC=RCV000014272.23; RCV000033554.2; RCV000014273.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen; MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1383:C0175704; CN166718; NBK1124:C0041409:163950:648
}}