{{Rsnum
|rsid=121918462
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTPN11
|position=112450398
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918462
|variant=0011
}}{{ClinVar
|rsid=121918462
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=112888202
|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
|CLNHGVS=NC_000012.11:g.112888202C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176876.0011; 176876.0013
|CLNSIG=5
|CLNCUI=C0041409
|CLNDBN=Noonan syndrome 1; Juvenile myelomonocytic leukemia; Noonan's syndrome; Rasopathy
|Disease=Noonan syndrome 1; Juvenile myelomonocytic leukemia; Noonan's syndrome; Rasopathy
|CLNACC=RCV000014262.22; RCV000030619.1; RCV000033475.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT; MedGen
|CLNDSDBID=NBK1124:C0041409:163950:648; C0349639:607785:86834; NBK1124:C0028326:163950:205824006; CN166718
}}