{{Rsnum
|rsid=121918453
|Chromosome=12
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PTPN11
|position=112450394
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918453
|variant=0001
}}{{ClinVar
|rsid=121918453
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=112888198
|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.112888198G>C; NC_000012.11:g.112888198G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176876.0001
|CLNSIG=5
|CLNCUI=C0041409
|CLNDBN=Rasopathy; Noonan's syndrome; Noonan syndrome 1
|Disease=Rasopathy; Noonan's syndrome; Noonan syndrome 1
|CLNACC=RCV000033472.2; RCV000037635.1; RCV000014252.22; RCV000033471.2; RCV000037636.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN166718; NBK1124:C0028326:163950:205824006; NBK1124:C0041409:163950:648
}}