{{Rsnum
|rsid=121918322
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FGF9
|position=21681060
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGF9
}}{{omim
|id=600921
|rsnum=121918322
|variant=0001
}}{{ClinVar
|rsid=121918322
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=22255199
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGF9:2254
|GENE_NAME=FGF9
|GENE_ID=2254
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.22255199G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600921.0001
|CLNSIG=5
|CLNCUI=C2751826
|CLNDBN=Multiple synostoses syndrome 3
|Disease=Multiple synostoses syndrome 3
|CLNACC=RCV000009242.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751826:612961:3237
}}