{{Rsnum
|rsid=121918504
|Chromosome=10
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FGFR2
|position=121517460
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=121918504
|variant=0028
}}{{ClinVar
|rsid=121918504
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=123276974
|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.123276974C>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000014212.16
|CLNDBN=Craniosynostosis, nonsyndromic unicoronal
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176943.0028
|Disease=Craniosynostosis
}}