Variant: rs67142165

present in Gene: EPHB2 present in Chromosome: 1 Position on Chromosome: 22884066 Alleles of this Variant: C/T

rs67142165 in EPHB2 gene and Thyroxine measurement PMID 30843173 2019 Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.

rs67142165 in EPHB2 gene and Triiodothyronine measurement PMID 30843173 2019 The EPHB2 gene variant rs67142165 reached genome-wide significance for association with fT3 plasma levels (P = 9.27 × 10<sup>-9</sup>) and its significance was confirmed in bivariate analysis (P = 9.72 × 10<sup>-9</sup>).