{{Rsnum
|rsid = 28933406
|Gene = HRAS
|geno1 = (A;A)
|geno2 = (A;C)
|geno3 = (C;C)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|Chromosome=11
|position=533875
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
}}NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

{{omim
|desc=THYROID CARCINOMA, FOLLICULAR, SOMATIC
|id=190020
|rsnum=28933406
|variant=0002
}}

{{ClinVar
|rsid=28933406
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=533875
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050260000000000002110120
|GENEINFO=HRAS:3265
|GENE_NAME=HRAS
|GENE_ID=3265
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.533875G>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000013434.1; RCV000022795.1
|CLNDBN=Thyroid carcinoma, follicular, somatic; Spermatocytic seminoma, somatic
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=190020.0002
|Disease=Thyroid carcinoma; Spermatocytic seminoma
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}