RS5912838 Unknown gene

Other Chr X:79241621
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What This Variant Does
"[GWAS:Graves' disease]"
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Graves' disease — OR: 1.32 2E-33 PubMed
Thyrotoxic hypokalemic periodic paralysis and Graves disease — OR: 1.62 6E-8 PubMed
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