rs10759944, PTCSC2

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.710 GeneticVariation BEFREE FOXE1 variants, associated with hypothyroidism, were not genome-wide significant (rs10759944: p = 1.08×10-6, β = -0.05). 25436638 2014
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.710 GeneticVariation GWASDB Novel associations for hypothyroidism include known autoimmune risk loci. 22493691 2012
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.710 GeneticVariation GWASDB Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. 21981779 2011
Thyroid stimulating hormone measurement
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
0.700 GeneticVariation GWASCAT Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. 25436638 2014
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
0.700 GeneticVariation GWASDB Genome-wide association study on differentiated thyroid cancer. 23894154 2013
Polysomnography
CUI: C0162701
Disease: Polysomnography
0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
0.700 GeneticVariation GWASDB The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. 20350937 2010
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
0.700 GeneticVariation GWASDB Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. 19198613 2009