Variant: rs191759494 

    present in Gene: DUOX2
    present in Chromosome: 15
    Position on Chromosome: 45108159
    Alleles of this Variant: C/G;T

rs191759494 in DUOX2 gene and Familial thyroid dyshormonogenesis PMID 21900383 2011 Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patients.

PMID 25248169 2014 High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands.

PMID 23457309 2013 Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene.

PMID 27821020 2017 DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin Phenotype.

PMID 26709262 2016 DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.

rs191759494 in DUOX2 gene and Thyroid Dyshormonogenesis 6 PMID 21900383 2011 Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patients.

PMID 27821020 2017 DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin Phenotype.

PMID 25248169 2014 High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands.

PMID 26709262 2016 DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.

PMID 23457309 2013 Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene.