{{Rsnum
|rsid=80338796
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAF1
|position=12604200
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAF1
}}{{omim
|id=164760
|rsnum=80338796
|variant=0001
}}{{ClinVar
|rsid=80338796
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=12645699
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=RAF1:5894
|GENE_NAME=RAF1
|GENE_ID=5894
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.12645699G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1383; 164760.0001
|CLNSIG=5
|CLNCUI=C1969057; C1969056; C0175704
|CLNDBN=Noonan syndrome 5; LEOPARD syndrome 2; LEOPARD syndrome
|Disease=Noonan syndrome 5; LEOPARD syndrome 2; LEOPARD syndrome
|CLNACC=RCV000014985.20; RCV000014986.20; RCV000020509.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen
|CLNDSDBID=NBK1124:C1969057:611553:648; NBK1383:C1969056:611554:500; NBK1383:C0175704
}}{{PMID Auto
|PMID=17603483
|Title=Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
}}