{{Rsnum
|rsid=121917756
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HRAS
|position=533869
|Gene_s=HRAS
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
}}{{omim
|id=190020
|rsnum=121917756
|variant=0009
}}{{ClinVar
|rsid=121917756
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=533869
|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.533869C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000013442.21
|CLNDBN=Myopathy, congenital, with excess of muscle spindles
|CLNDSDB=MedGen
|CLNDSDBID=C1968782
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=190020.0009
|Disease=Myopathy
}}