rs944289, None

N. diseases: 16
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.050 GeneticVariation BEFREE Association of rs944289, which was previously known to confer risk for thyroid cancer, with FA, and the correlation between PTCSC3 and NRG1 expression demonstrates that predisposing genetic factors are partly common for benign and malignant thyroid tumors, and imply broader roles of the pathways they underlie in thyroid tumorigenesis, not limited to carcinogenesis. 25562676 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.050 GeneticVariation BEFREE Overall, meta-analysis of rs944289</span> showed 1.11-fold increased risk of thyroid cancer related to the risk T allele (T vs. C: OR 1.11, 95 % CI 1.05-1.17). 26206751 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.050 GeneticVariation BEFREE Our result demonstrated that rs9442</span>89 polymorphism on 14q13.3 is a low penetrant risk factor for developing TC. 25552255 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.050 GeneticVariation BEFREE Five single nucleotide polymorphisms (SNPs) were previously reported to be associated with thyroid cancer in European populations in two genome-wide association studies (GWAS): rs965513 (9q22.33), rs944289 (14q13.3), rs116909374 (14q13.3), rs966423 (2q35) and rs2439302 (8p12). 23847140 2013
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
0.050 GeneticVariation BEFREE Five single nucleotide polymorphisms (SNPs) associated with thyroid cancer (TC) risk have been reported: rs2910164 (5q24); rs6983267 (8q24); rs965513 and rs1867277 (9q22); and rs944289 (14q13). 22282540 2012