{{Rsnum
|rsid=121918677
|Gene=TF
|Chromosome=3
|position=133777188
|Orientation=plus
|GMAF=0.003214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TF
}}{{omim
|id=190000
|rsnum=121918677
|variant=0003
}}{{ClinVar
|rsid=121918677
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=133496032
|CHROM=3
|GMAF=0.0032
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=TF:7018
|GENE_NAME=TF
|GENE_ID=7018
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.133496032G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9968; 0.003214
|CLNACC=RCV000013450.21
|CLNDBN=Transferrin variant b2
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=190000.0003
|COMMON=1
|Disease=Transferrin variant b2
}}