{{Rsnum
|rsid=121434497
|Chromosome=19
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MAP2K2
|position=4117552
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAP2K2
}}{{omim
|id=601263
|rsnum=121434497
|variant=0001
}}{{ClinVar
|rsid=121434497
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=4117550
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MAP2K2:5605
|GENE_NAME=MAP2K2
|GENE_ID=5605
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.4117550A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601263.0001
|CLNSIG=5
|CLNCUI=C1275081
|CLNDBN=Cardiofaciocutaneous syndrome 4
|Disease=Cardiofaciocutaneous syndrome 4
|CLNACC=RCV000008761.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN176914:615280:1340
}}