Normal allele: GG
Genetic determinants of body iron stores and risk of type 2 diabetes.
Polymorphism rs3811647 is related to topics like this:
Research and publications:
19084217 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.
19820699 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.
21483845 Genome-wide association study identifies genetic loci associated with iron deficiency.
21665994 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.
22815867 Genetic determinants for body iron store and type 2 diabetes risk in US men and women.
23903878 Prenatal methylmercury exposure and genetic predisposition to cognitive deficit at age 8 years.
23996192 Toenail iron, genetic determinants of iron status, and the risk of glioma.
24391736 The contribution of diet and genotype to iron status in women: a classical twin study.
27255824 Determinants of iron accumulation in the normal aging brain.
27730450 Candidate gene studies of diabetic retinopathy in human.
29942042 A decade in psychiatric GWAS research.
33758941 Genetics of Iron Metabolism and Premenstrual Symptoms: A Mendelian Randomization Study.
34666587 Placental cadmium, placental genetic variations, and birth size.
24121126 Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin.