{{Rsnum
|rsid=121918505
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGFR2
|position=121520119
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR2
}}{{omim
|id=176943
|rsnum=121918505
|variant=0029
}}{{ClinVar
|rsid=121918505
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=123279633
|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.123279633A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176943.0029
|CLNSIG=255
|CLNCUI=C1863356
|CLNDBN=Pfeiffer syndrome; Neoplasm of stomach
|Disease=Pfeiffer syndrome; Neoplasm of stomach
|CLNACC=RCV000014213.23; RCV000014214.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1455:C1863356:101600:710; C0038356:613659:63443:126824007
}}