{{Rsnum
|rsid=387906676
|Chromosome=10
|position=121517394
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FGFR2
|Gene_s=FGFR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=10
|CLNACC=RCV000022732.23; RCV000022733.1
|CLNALLE=1; 2
|CLNDBN=Crouzon syndrome; Variant of unknown significance
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1455:C0010273:123500:207:28861008
|CLNHGVS=NC_000010.10:g.123276908C>G; NC_000010.10:g.123276908C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176943.0041; 176943.0042
|Disease=Crouzon syndrome; Variant of unknown significance
|FwdALT=A,C
|FwdREF=G
|REF=C
|RSPOS=123276908
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906676
|GENEINFO=FGFR2:2263
|GENE_ID=2263
|GENE_NAME=FGFR2
}}