{{Rsnum
|rsid=267606990
|Orientation=plus
|Chromosome=12
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTPN11
|position=112419116
|Gene_s=PTPN11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000014277.1; RCV000033445.2; RCV000037652.1
|CLNALLE=1
|CLNDBN=Noonan syndrome 1; Rasopathy; Noonan's syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1124:C0041409:163950:648; CN166718; NBK1124:C0028326:163950:205824006
|CLNHGVS=NC_000012.11:g.112856920C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176876.0027
|Disease=Noonan syndrome 1; Rasopathy; Noonan's syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=PTPN11:5781
|GENE_ID=5781
|GENE_NAME=PTPN11
|REF=C
|RSPOS=112856920
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606990
}}