Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs179247
rs179247
Entrez Id: 7253
Gene Symbol: TSHR
TSHR
CUI: C0040128
Disease:
Thyroid Diseases
0.010 GeneticVariation BEFREE Analysis of chosen polymorphisms rs2476601 a/G - PTPN22, rs1990760 C/T - IFIH1, rs179247 a/G - TSHR in pathogenesis of autoimmune thyroid diseases in children. 29973096 2018