{{Rsnum
|rsid=121918463
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTPN11
|position=112477651
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918463
|variant=0012
}}{{ClinVar
|rsid=121918463
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=112915455
|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.112915455T>C; NC_000012.11:g.112915455T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176876.0012
|CLNSIG=5
|CLNCUI=C0041409
|CLNDBN=Noonan syndrome 1; Rasopathy; Noonan's syndrome; not provided
|Disease=Noonan syndrome 1; Rasopathy; Noonan's syndrome; not provided
|CLNACC=RCV000014263.16; RCV000033514.3; RCV000037663.1; RCV000077862.1; RCV000033513.2; RCV000037664.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1124:C0041409:163950:648; CN166718; NBK1124:C0028326:163950:205824006
}}