rs3184504, SH2B3;ATXN2

N. diseases: 92
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.800 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.800 GeneticVariation GWASCAT Novel associations for hypothyroidism include known autoimmune risk loci. 22493691 2012
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.800 GeneticVariation GWASDB Novel associations for hypothyroidism include known autoimmune risk loci. 22493691 2012