{{Rsnum
|rsid=121918214
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FTO
|position=53873837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FTO
}}{{omim
|id=610966
|rsnum=121918214
|variant=0001
}}{{ClinVar
|rsid=121918214
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=53907749
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FTO:79068
|GENE_NAME=FTO
|GENE_ID=79068
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.53907749G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610966.0001
|CLNSIG=5
|CLNCUI=C2752001
|CLNDBN=Growth retardation, developmental delay, coarse facies, and early death
|Disease=Growth retardation
|CLNACC=RCV000001110.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2752001:612938:210144
}}