DIO2, iodothyronine deiodinase 2, 1734

N. diseases: 79; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs225014
rs225014
Entrez Id: 1734
Gene Symbol: DIO2
DIO2
CUI: C0018213
Disease:
Graves Disease
0.030 GeneticVariation BEFREE Seven SNPs in the DIO2 gene - rs225014 (Thr92Ala), rs12885300, rs2267872, rs225011, rs224995, rs225015, and rs2267873 - were studied to assess their association with GD and GO. 30574458 2018
dbSNP: rs225014
rs225014
Entrez Id: 1734
Gene Symbol: DIO2
DIO2
CUI: C0018213
Disease:
Graves Disease
0.030 GeneticVariation BEFREE Type 2 deiodinase Thr92Ala polymorphism impact on clinical course and myocardial remodeling in patients with Graves' disease. 19684474 2009
dbSNP: rs225014
rs225014
Entrez Id: 1734
Gene Symbol: DIO2
DIO2
CUI: C0018213
Disease:
Graves Disease
0.030 GeneticVariation BEFREE This suggests that the Thr92Ala variant of the DIO2 gene is associated or may be in linkage disequilibrium with a functional DIO2 polymorphism which involves in the development of GD in a Russian population. 15542398 2004
dbSNP: rs12885300
rs12885300
Entrez Id: 1734;100628307
Gene Symbol: DIO2;DIO2-AS1
DIO2;DIO2-AS1
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE Therefore, we genotyped D1 rs11206244, D2 rs225014, and rs12885300 polymorphisms in 134 GD patients, including 54 patients with intractable GD and 44 patients with GD in remission and 132 HD patients, including 57 patients with severe HD, 45 patients with mild HD, and 84 healthy controls using PCR-RFLP. 29648895 2018
dbSNP: rs2267873
rs2267873
Entrez Id: 1734
Gene Symbol: DIO2
DIO2
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE Seven SNPs in the DIO2 gene - rs225014 (Thr92Ala), rs12885300, rs2267872, rs225011, rs224995, rs225015, and rs2267873 - were studied to assess their association with GD and GO. 30574458 2018