{{Rsnum
|rsid=267607230
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MAP2K2
|position=4110576
|Gene_s=MAP2K2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000008764.3
|CLNALLE=1
|CLNDBN=Cardiofaciocutaneous syndrome 4
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN176914:615280:1340
|CLNHGVS=NC_000019.9:g.4110574G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601263.0004
|Disease=Cardiofaciocutaneous syndrome 4
|FwdALT=A
|FwdREF=C
|GENEINFO=MAP2K2:5605
|GENE_ID=5605
|GENE_NAME=MAP2K2
|REF=G
|RSPOS=4110574
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607230
}}