{{Rsnum
|rsid=80338797
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RAF1
|position=12584624
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAF1
}}{{omim
|id=164760
|rsnum=80338797
|variant=0004
}}{{ClinVar
|rsid=80338797
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=12626123
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=RAF1:5894
|GENE_NAME=RAF1
|GENE_ID=5894
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.12626123G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1383; 164760.0004
|CLNSIG=5
|CLNCUI=C1969056; C1969057; C0175704
|CLNDBN=LEOPARD syndrome 2; Noonan syndrome 5; LEOPARD syndrome; Noonan's syndrome
|Disease=LEOPARD syndrome 2; Noonan syndrome 5; LEOPARD syndrome; Noonan's syndrome
|CLNACC=RCV000014989.24; RCV000014990.20; RCV000020508.1; RCV000037683.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1383:C1969056:611554:500; NBK1124:C1969057:611553:648; NBK1383:C0175704; NBK1124:C0028326:163950:205824006
}}{{PMID Auto
|PMID=17603482
|Title=Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
}}

{{PMID Auto
|PMID=17603483
|Title=Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
}}