Variant: rs10759944 

    present in Gene: PTCSC2
    present in Chromosome: 9
    Position on Chromosome: 97794690
    Alleles of this Variant: A/G

rs10759944 in PTCSC2 gene and Hypothyroidism PMID 21981779 2011 Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.

PMID 22493691 2012 Novel associations for hypothyroidism include known autoimmune risk loci.

rs10759944 in PTCSC2 gene and Polysomnography PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs10759944 in PTCSC2 gene and Thyroid carcinoma PMID 19198613 2009 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.

PMID 20350937 2010 The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.

PMID 23894154 2013 Genome-wide association study on differentiated thyroid cancer.

rs10759944 in PTCSC2 gene and Thyroid stimulating hormone measurement PMID 25436638 2014 Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.