{{Rsnum
|rsid=121434594
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAF1
|position=12604189
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAF1
}}{{omim
|id=164760
|rsnum=121434594
|variant=0002
}}{{ClinVar
|rsid=121434594
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=12645688
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110104
|GENEINFO=RAF1:5894
|GENE_NAME=RAF1
|GENE_ID=5894
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000003.11:g.12645688G>A; NC_000003.11:g.12645688G>C; NC_000003.11:g.12645688G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164760.0002
|CLNSIG=5
|CLNCUI=C1969057
|CLNDBN=Noonan syndrome 5; Noonan's syndrome
|Disease=Noonan syndrome 5; Noonan's syndrome
|CLNACC=RCV000014987.24; RCV000037705.1; RCV000037704.1; RCV000037703.1
|Tags=RV;PM;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1124:C1969057:611553:648; NBK1124:C0028326:163950:205824006
}}