{{Rsnum
|rsid=121918491
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FGFR2
|position=121517371
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=121918491
|variant=0006
}}{{ClinVar
|rsid=121918491
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=123276885
|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
|CLNHGVS=NC_000010.10:g.123276885C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176943.0006
|CLNSIG=5
|CLNCUI=C0010273
|CLNDBN=Crouzon syndrome; Craniosynostosis, nonclassifiable autosomal dominant; Scaphocephaly and axenfeld-rieger anomaly
|Disease=Crouzon syndrome; Craniosynostosis; Scaphocephaly and axenfeld-rieger anomaly
|CLNACC=RCV000014184.22; RCV000014185.16; RCV000014186.23
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1455:C0010273:123500:207:28861008
}}