RS4947296 Unknown gene

Other Chr 6:31090401
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What This Variant Does
"rs4947296 is considered to be a SNP in the MUC21 gene, located upstream of the HLA locus on chromoso..."
GWAS Studies (4)
Trait Risk Allele OR / Beta P-value Study
Graves' disease C OR: 1.77 4E-51 PubMed
Thyrotoxic hypokalemic periodic paralysis and Graves disease — OR: 2.06 3E-22 PubMed
Behcet's disease — OR: 2.57 1E-11 PubMed
Nasopharyngeal carcinoma (SNP x SNP interaction) G — 8E-9 PubMed
Ask Dr. Hemsworth about this variant