{{Rsnum
|rsid=397507549
|Chromosome=12
|position=112489104
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PTPN11
|Gene_s=PTPN11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,G
|CHROM=12
|CLNACC=RCV000033552.2; RCV000033553.2; RCV000055888.1
|CLNALLE=1; 2
|CLNDBN=Rasopathy; LEOPARD syndrome 1
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN166718; NBK1383:CN074218:151100:500
|CLNHGVS=NC_000012.11:g.112926908C>A; NC_000012.11:g.112926908C>G
|CLNSIG=5
|Disease=Rasopathy; LEOPARD syndrome 1
|FwdALT=A,G
|FwdREF=C
|REF=C
|RSPOS=112926908
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=397507549
|CLNSRC=GeneReviews
|CLNSRCID=NBK1383
|GENEINFO=PTPN11:5781
|GENE_ID=5781
|GENE_NAME=PTPN11
}}