{{Rsnum
|rsid=121918471
|Chromosome=12
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GGT)
|geno3=(GGT;GGT)
|Gene=PTPN11
|position=112450358
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTPN11
}}{{omim
|id=176876
|rsnum=121918471
|variant=0024
}}{{ClinVar
|rsid=121918471
|Reversed=0
|FwdREF=GGT
|FwdALT=
|REF=TGGT
|ALT=T
|RSPOS=112888161
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050060000001000002110200
|GENEINFO=PTPN11:5781
|GENE_NAME=PTPN11
|GENE_ID=5781
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.112888162_112888164delGGT
|CLNSRC=OMIM Allelic Variant; GeneReviews
|CLNORIGIN=1
|CLNSRCID=176876.0024; 176876.0024; NBK1124; NBK1124
|CLNSIG=1
|CLNCUI=C0041409; C0041409; C0041409; C0041409
|CLNDBN=Noonan syndrome 1
|Disease=Noonan syndrome 1
|CLNACC=SCV000034523.1; SCV000034523.1; SCV000040936.1; SCV000040936.1
|Tags=PM;OTHERKG;LSD;OM
}}