RS10759944 Unknown gene

Other Chr 9:97794690
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What This Variant Does
"Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer"
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Serum thyroid-stimulating hormone levels A β: 0.05 1E-6 PubMed
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