{{Rsnum
|rsid=121909627
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FGFR1
|position=38424690
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGFR1
}}{{omim
|id=136350
|rsnum=121909627
|variant=0001
}}{{ClinVar
|rsid=121909627
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=38282208
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FGFR1:2260
|GENE_NAME=FGFR1
|GENE_ID=2260
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.38282208G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=136350.0001
|CLNSIG=5
|CLNCUI=C1863356; C0795998
|CLNDBN=Pfeiffer syndrome; Jackson-Weiss syndrome
|Disease=Pfeiffer syndrome; Jackson-Weiss syndrome
|CLNACC=RCV000017669.26; RCV000017670.26
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1455:C1863356:101600:710; NBK1455:C0795998:123150:1540
}}