{{Rsnum
|rsid=121918488
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR2
|position=121517379
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=121918488
|variant=0003
}}{{ClinVar
|rsid=121918488
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=123276893
|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.123276893A>G; NC_000010.10:g.123276893A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176943.0002; 176943.0003
|CLNSIG=5
|CLNCUI=C0010273; C1863356; C0795998,C0010273; C0795998
|CLNDBN=Crouzon syndrome; Pfeiffer syndrome; Jackson-Weiss syndrome; Antley-bixler syndrome without genital anomalies or disordered steroidogenesis
|Disease=Crouzon syndrome; Pfeiffer syndrome; Jackson-Weiss syndrome; Antley-bixler syndrome without genital anomalies or disordered steroidogenesis
|CLNACC=RCV000014177.22; RCV000014178.23; RCV000014179.22; RCV000014180.23; RCV000014181.24; RCV000014182.22; RCV000014183.16
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1455:C0010273:123500:207:28861008; NBK1455:C1863356:101600:710; NBK1455:C0795998:123150:1540
}}