{{Rsnum
|rsid=121918498
|Chromosome=10
|Orientation=minus
|geno1=(CG;CG)
|geno2=(CG;TT)
|geno3=(TT;TT)
|Gene=FGFR2
|position=121520162
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=121918498
|variant=0017
}}{{ClinVar
|rsid=121918498
|Reversed=1
|FwdREF=CG
|FwdALT=TT
|REF=GCG
|ALT=GAA
|RSPOS=123279675
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110800
|GENEINFO=FGFR2:2263
|GENE_NAME=FGFR2
|GENE_ID=2263
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.123279676_123279677delCGinsAA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176943.0017; 176943.0026
|CLNSIG=5
|CLNCUI=C0001193
|CLNDBN=Acrocephalosyndactyly type I
|Disease=Acrocephalosyndactyly type I
|CLNACC=RCV000014201.23
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1455:C0001193:101200:87:205258009
}}