{{Rsnum
|rsid=104894229
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HRAS
|position=534289
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=190020
|rsnum=104894229
|variant=0003
}}
{{omim
|id=190020
|rsnum=104894229
|variant=0014
}}{{ClinVar
|rsid=104894229
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=534289
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050260000000000002110124
|GENEINFO=HRAS:3265
|GENE_NAME=HRAS
|GENE_ID=3265
|WGT=0
|VC=SNV
|CLNALLE=1; 3
|CLNHGVS=NC_000011.9:g.534289C>A; NC_000011.9:g.534289C>T
|CLNSRC=OMIM Allelic Variant; Emory University
|CLNORIGIN=2; 1
|CLNSRCID=190020.0014; 9898; 190020.0003
|CLNSIG=255
|CLNCUI=C0587248
|CLNDBN=Costello syndrome; NEVUS SEBACEOUS, SOMATIC; Nevus, epidermal, somatic; Myopathy, congenital, with excess of muscle spindles; EPIDERMAL NEVUS WITH UROTHELIAL CANCER, SOMATIC; not provided
|Disease=Costello syndrome; NEVUS SEBACEOUS; Nevus; Myopathy; EPIDERMAL NEVUS WITH UROTHELIAL CANCER; not provided
|CLNACC=RCV000013447.22; RCV000029211.1; RCV000032851.1; RCV000013435.24; RCV000013436.21; RCV000022796.1; RCV000029209.1; RCV000081295.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1507:C0587248:218040:3071:309776008; C1968782
}}