rs10759944, PTCSC2

N. diseases: 4
Disease: Hypothyroidism ×
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