{{Rsnum
|rsid=281865420
|Chromosome=10
|position=121520161
|Orientation=minus
|geno1=(CGC;CGC)
|geno2=(CGC;TCT)
|geno3=(TCT;TCT)
|Gene=FGFR2
|Gene_s=FGFR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=GAGA
|CHROM=10
|CLNACC=RCV000014202.22
|CLNALLE=1
|CLNDBN=Pfeiffer syndrome variant
|CLNHGVS=NC_000010.10:g.123279675_123279677delGCGinsAGA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176943.0018
|Disease=Pfeiffer syndrome variant
|FwdALT=TCT
|FwdREF=CGC
|REF=GGCG
|RSPOS=123279674
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=MNV
|VP=0x050060000000000002110800
|WGT=0
|dbSNPBuildID=137
|rsid=281865420
|GENEINFO=FGFR2:2263
|GENE_ID=2263
|GENE_NAME=FGFR2
}}