Variant: rs965513 

    present in Gene: PTCSC2
    present in Chromosome: 9
    Position on Chromosome: 97793827
    Alleles of this Variant: A/G;T

rs965513 in PTCSC2 gene and Hypothyroidism PMID 22493691 2012 Novel associations for hypothyroidism include known autoimmune risk loci.

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

rs965513 in PTCSC2 gene and Nasopharyngeal carcinoma PMID 20512145 2010 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.

rs965513 in PTCSC2 gene and Polysomnography PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs965513 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 22267200 2012 Of those, rs965513 has previously been shown to associate with thyroid cancer.

PMID 25855579 2015 Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations.

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