{{Rsnum
|rsid=104894231
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HRAS
|position=533467
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=190020
|rsnum=104894231
|variant=0008
}}{{ClinVar
|rsid=104894231
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=533467
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HRAS:3265
|GENE_NAME=HRAS
|GENE_ID=3265
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.533467C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=190020.0008
|CLNSIG=5
|CLNCUI=C0587248
|CLNDBN=Costello syndrome
|Disease=Costello syndrome
|CLNACC=RCV000013441.15
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1507:C0587248:218040:3071:309776008
}}