{{Rsnum
|rsid=2692696
|Gene=TF
|Chromosome=3
|position=133766289
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.007805
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 86.2 | 13.8 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2692696
|allele=G
|frequency=1
|uid=1103656233842
|type=homozygous_SNP
|hugo=TF
|ensembl gene=ENSG00000091513
|ensembl transcript=ENST00000264998
|sift=TOLERATED
|disease=Defects in TF are the cause of atransferrinemia (MIM:209300). Atransferrinemia is rare autosomal recessive disorder characterized by iron overload and hypochromic anemia.
}}

{{GET Evidence
|gene=TF
|aa_change=Ile448Val
|aa_change_short=I448V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2692696
|overall_frequency_n=10752
|overall_frequency_d=10758
|overall_frequency=0.999442
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=111
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}