rs1799852 is a SNP in the TF gene. It is significantly associated with serum transferrin concentrations [R].

The minor allele ''T'' is related to lower circulating serum transferrin levels in menstruating women [R].

rs1799852

Parent Gene: TF

Importance: 2
Less common allele: T = 14%
More common allele: C = 86%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Iron Biomarker Measurement

rs1799852 is associated with Iron Biomarker Measurement (R) . It is reported to have a 0.43 s.d. decrease on Iron status biomarkers (serum transferrin). No specific risk allele was identified in the study.

Disease/Trait: Iron Biomarker Measurement

The T allele of rs1799852 is reported to be associated with Iron Biomarker Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Iron status biomarkers (transferrin saturation).

Disease/Trait: Transferrin Saturation Measurement

The T allele of rs1799852 is reported to be associated with Transferrin Saturation Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Iron status biomarkers (transferrin saturation).