{{Rsnum
|rsid=80338799
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAF1
|position=12585745
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAF1
}}{{omim
|id=164760
|rsnum=80338799
|variant=0003
}}{{ClinVar
|rsid=80338799
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=12627244
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=RAF1:5894
|GENE_NAME=RAF1
|GENE_ID=5894
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.12627244G>A; NC_000003.11:g.12627244G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0; 1
|CLNSRCID=NBK1383; 164760.0003
|CLNSIG=5
|CLNCUI=C0175704; C1969057
|CLNDBN=LEOPARD syndrome; Noonan's syndrome; Noonan syndrome 5
|Disease=LEOPARD syndrome; Noonan's syndrome; Noonan syndrome 5
|CLNACC=RCV000020507.1; RCV000037676.1; RCV000014988.24
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen; GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1383:C0175704; NBK1124:C0028326:163950:205824006; NBK1124:C1969057:611553:648
}}