{{Rsnum
|rsid=267606920
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NRAS
|position=114713911
|Gene_s=NRAS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000014917.24
|CLNALLE=1
|CLNDBN=Noonan syndrome 6
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1124:C2750732:613224:ORPHA648
|CLNHGVS=NC_000001.11:g.114713911C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_002524.4:c.179G>A; 164790.0005
|Disease=Noonan syndrome 6
|FwdALT=A
|FwdREF=G
|GENEINFO=NRAS:4893
|GENE_ID=4893
|GENE_NAME=NRAS
|REF=C
|RSPOS=114713911
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267606920
|CLNORIGIN=1
}}