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SNP information rs236918

RS236918

Normal allele: GG

Polymorphism rs236918 is related to topics like this:

Genetic haemochromatosis

Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...


Research and publications:

  21149283   Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.

  23996192   Toenail iron, genetic determinants of iron status, and the risk of glioma.

  24396277   Genetics of the first seven proprotein convertase enzymes in health and disease.

  24556216   Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis.

  25504030   PCSK7 genotype modifies effect of a weight-loss diet on 2-year changes of insulin resistance: the POUNDS LOST trial.

  27437086   Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences.

  28338112   PNPLA3 and RNF7 Gene Variants are Associated with the Risk of Developing Liver Fibrosis and Cirrhosis in an Eastern European Population.

  29167213   Interaction of Dietary and Genetic Factors Influencing Body Iron Status and Risk of Type 2 Diabetes Within the EPIC-InterAct Study.

  30918065   PCSK7 gene variation bridges atherogenic dyslipidemia with hepatic inflammation in NAFLD patients.

  33170161   Genetic test for the prescription of diets in support of physical activity.

  33565643   Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis.

  34207761   The rs508487, rs236911, and rs236918 Genetic Variants of the Proprotein Convertase Subtilisin-Kexin Type 7 (PCSK7) Gene Are Associated with Acute Coronary Syndrome and with Plasma Concentrations of HDL-Cholesterol and Triglycerides.

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CCNB1 cyclin B1

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