{{Rsnum
|rsid=121918499
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FGFR2
|position=121520048
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=121918499
|variant=0019
}}{{ClinVar
|rsid=121918499
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=123279562
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FGFR2:2263
|GENE_NAME=FGFR2
|GENE_ID=2263
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000010.10:g.123279562C>A; NC_000010.10:g.123279562C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176943.0032; 176943.0019
|CLNSIG=5
|CLNCUI=C1863356
|CLNDBN=Pfeiffer syndrome; Craniofacial-skeletal-dermatologic dysplasia
|Disease=Pfeiffer syndrome; Craniofacial-skeletal-dermatologic dysplasia
|CLNACC=RCV000014217.23; RCV000014218.23; RCV000014203.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1455:C1863356:101600:710
}}