RS10504861 Unknown gene
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What This Variant Does
"rs10504861 is a SNP located on Chromosome 8q21 that was found to be associated with elevated inciden..."
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Migraine without aura | — | OR: 1.16 | 1E-8 | PubMed |