{{Rsnum
|rsid=77543610
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FGFR2
|position=121520160
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=77543610
|variant=0011
}}{{ClinVar
|rsid=77543610
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=123279674
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000000402110100
|GENEINFO=FGFR2:2263
|GENE_NAME=FGFR2
|GENE_ID=2263
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.123279674G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176943.0011
|CLNSIG=5
|CLNCUI=C0001193
|CLNDBN=Acrocephalosyndactyly type I
|Disease=Acrocephalosyndactyly type I
|CLNACC=RCV000014193.23
|Tags=PM;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1455:C0001193:101200:87:205258009
}}