{{Rsnum
|rsid=121908595
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MAP2K1
|position=66436843
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAP2K1
}}{{omim
|id=176872
|rsnum=121908595
|variant=0002
}}{{ClinVar
|rsid=121908595
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=66729181
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MAP2K1:5604
|GENE_NAME=MAP2K1
|GENE_ID=5604
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.66729181A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176872.0002
|CLNSIG=5
|CLNCUI=C1275081
|CLNDBN=Cardio-facio-cutaneous syndrome; Cardiofaciocutaneous syndrome 3
|Disease=Cardio-facio-cutaneous syndrome; Cardiofaciocutaneous syndrome 3
|CLNACC=RCV000014279.3; RCV000043672.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1186:C1275081:115150:1340:403770008; CN176913:615279:1340
}}