{{Rsnum
|rsid=121918461
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PTPN11
|position=112450362
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918461
|variant=0010
}}{{ClinVar
|rsid=121918461
|Reversed=0
|FwdREF=A
|FwdALT=G,T
|REF=A
|ALT=G,T
|RSPOS=112888166
|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.112888166A>G; NC_000012.11:g.112888166A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176876.0010
|CLNSIG=5
|CLNCUI=C0041409
|CLNDBN=Noonan syndrome 1; Rasopathy; not provided
|Disease=Noonan syndrome 1; Rasopathy; not provided
|CLNACC=RCV000014258.23; RCV000033464.3; RCV000077856.1; RCV000033465.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1124:C0041409:163950:648; CN166718
}}