{{Rsnum
|rsid=104894228
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HRAS
|position=534286
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=190020
|rsnum=104894228
|variant=0007
}}{{ClinVar
|rsid=104894228
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=534286
|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; 2
|CLNHGVS=NC_000011.9:g.534286C>A; NC_000011.9:g.534286C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1; 2
|CLNSRCID=190020.0007; 190020.0017
|CLNSIG=255
|CLNCUI=C0587248
|CLNDBN=Costello syndrome; NEVUS SEBACEOUS, SOMATIC; SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME, SOMATIC MOSAIC; Nevus, epidermal, somatic
|Disease=Costello syndrome; NEVUS SEBACEOUS; SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; Nevus
|CLNACC=RCV000013440.23; RCV000029212.1; RCV000029213.1; RCV000032852.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1507:C0587248:218040:3071:309776008
}}