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SNP information rs9606756

RS9606756

Normal allele: AA

Polymorphism associated with serum levels of vitamin B12. Also associated with transcobalamin concentrations in pregnant women and risk of neural tube defects in the foetus.

Polymorphism rs9606756 is related to topics like this:

Mthfr and B12

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DNA methylation genes

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Research and publications:

  12107818   Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects.

  16400609   Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing.

  18203168   Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts

  21615938   Genetic polymorphisms in folate pathway enzymes, DRD4 and GSTM1 are related to temporomandibular disorder.

  21857689   Folate and vitamin B12 in idiopathic male infertility.

  21865561   Transcobalamin polymorphism 67A->G, but not 776C->G, affects serum holotranscobalamin in a cohort of healthy middle-aged men and women.

  21975197   Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk.

  22116453   Folate and vitamin B12-related genes and risk for omphalocele.

  22496743   Genetic variant of AMD1 is associated with obesity in urban Indian children.

  22792358   Association between genetic variants in DNA and histone methylation and telomere length.

  23227234   Vitamin B-12 status during pregnancy and child IQ at 8 years of age: a Mendelian randomized trial within the Avon Parent-Child Longitudinal Study.

  23552396   Genetic and non-genetic predictors of LINE-1 methylation in leukocyte DNA.

  24130171   Global DNA methylation and one-carbon metabolism gene polymorphisms and the risk of breast cancer in the Sister Study.

  24524080   The effect of multiple single nucleotide polymorphisms in the folic acid pathway genes on homocysteine metabolism.

  25681243   Single nucleotide polymorphisms related to vitamin B12 serum levels in autoimmune gastritis patients with or without pernicious anaemia.

  28417558   The TCN2 variant of rs9606756 [Ile23Val] acts as risk loci for obesity-related traits and mediates by interacting with Apo-A1.

  28472811   Analysis of transcobalamin II gene polymorphisms and serum homocysteine, folate and vitamin B12 levels in Chinese patients with Crohn's disease.

  28526947   Association of ulcerative colitis with transcobalamin II gene polymorphisms and serum homocysteine, vitamin B(12), and folate levels in Chinese patients.

  28981944   [Association of transcobalamine II gene polymorphisms and serum homocysteine, vitamin B(12) and folate levels with ulcerative colitis among Chinese patients].

  30108155   Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.

  32207595   Relationship between cobalt transporter II gene rs9606756 site mutant and serum homocysteine level and recurrent cerebral infarction in young and middle-aged people.

  33195260   Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.

  34131278   Genetic polymorphisms associated with obesity in the Arab world: a systematic review.

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