{{Rsnum
|rsid = 11554290
|Gene = NRAS
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=1
|position=114713908
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NRAS
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=THYROID CARCINOMA, FOLLICULAR
|id=164790
|rsnum=11554290
|variant=0002
}}

{{ClinVar
|rsid=11554290
|Reversed=1
|FwdREF=A
|FwdALT=C,G,T
|REF=T
|ALT=A,C,G
|RSPOS=114713908
|CHROM=1
|dbSNPBuildID=120
|SSR=0
|SAO=3
|VP=0x050360000a05040103110124
|GENEINFO=NRAS:4893
|GENE_NAME=NRAS
|GENE_ID=4893
|WGT=1
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000001.11:g.114713908T>C
|CLNORIGIN=2
|CLNSRCID=
NM_002524.4:c.182A>G; 164790.0002
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000014914.2; RCV000032847.2; RCV000037574.1; RCV000114744.1; RCV000114745.1
|Tags=RV;PM;S3D;SLO;NSM;REF;ASP;VLD;GNO;OTHERKG;PH3;LSD;OM;NOV
|CLNDBN=Thyroid carcinoma, follicular, somatic; Epidermal nevus; Non-small cell lung cancer; MELANOCYTIC NEVUS SYNDROME, CONGENITAL, SOMATIC; NEUROCUTANEOUS MELANOSIS, SOMATIC
|CLNDSDB=MedGen:OMIM:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=C0334082:162900:25201003; C0007131:254637007
|CLNSRC=ClinVar; OMIM Allelic Variant
|Disease=Thyroid carcinoma; Epidermal nevus; Non-small cell lung cancer; MELANOCYTIC NEVUS SYNDROME; NEUROCUTANEOUS MELANOSIS
}}

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