{{Rsnum
|rsid=121434596
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NRAS
|position=114716123
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NRAS
}}{{omim
|id=164790
|rsnum=121434596
|variant=0003
}}{{ClinVar
|rsid=121434596
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=114716123
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=3
|VP=0x050260000a05000002110124
|GENEINFO=NRAS:4893
|GENE_NAME=NRAS
|GENE_ID=4893
|WGT=1
|VC=SNV
|CLNALLE=3
|CLNHGVS=NC_000001.11:g.114716123C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NM_002524.4:c.38G>A; 164790.0003
|CLNCUI=.,.,CN069957; C0349639; C2750732
|CLNDBN=AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IV; Noonan syndrome 6
|Disease=AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; Noonan syndrome 6
|CLNACC=RCV000014915.24; RCV000022690.23
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C2674723:614470:ORPHA3261; NBK1124:C2750732:613224:ORPHA648
|CLNSIG=5
}}