{{Rsnum
|rsid=121434499
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MAP2K2
|position=4110559
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAP2K2
}}{{omim
|id=601263
|rsnum=121434499
|variant=0003
}}{{ClinVar
|rsid=121434499
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=4110557
|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.4110557A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601263.0003
|CLNSIG=5
|CLNCUI=C1275081
|CLNDBN=Cardio-facio-cutaneous syndrome; Cardiofaciocutaneous syndrome 4
|Disease=Cardio-facio-cutaneous syndrome; Cardiofaciocutaneous syndrome 4
|CLNACC=RCV000008763.3; RCV000043675.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1186:C1275081:115150:1340:403770008; CN176914:615280:1340
}}