{{Rsnum
|rsid=121908594
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MAP2K1
|position=66435104
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAP2K1
}}{{omim
|id=176872
|rsnum=121908594
|variant=0001
}}{{ClinVar
|rsid=121908594
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=66727442
|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.66727442T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176872.0001
|CLNSIG=5
|CLNCUI=C1275081
|CLNDBN=Cardiofaciocutaneous syndrome 3
|Disease=Cardiofaciocutaneous syndrome 3
|CLNACC=RCV000014278.25
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN176913:615279:1340
}}