{{Rsnum
|rsid=121918455
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PTPN11
|position=112477720
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918455
|variant=0004
}}{{ClinVar
|rsid=121918455
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=112915524
|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.112915524A>C; NC_000012.11:g.112915524A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176876.0004
|CLNSIG=5
|CLNCUI=C0041409
|CLNDBN=Rasopathy; Noonan's syndrome; Noonan syndrome 1
|Disease=Rasopathy; Noonan's syndrome; Noonan syndrome 1
|CLNACC=RCV000033517.2; RCV000037668.1; RCV000014255.24; RCV000033518.2; RCV000037669.1
|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
}}