RS4353135 Unknown gene

Other Chr 1:247453734
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What This Variant Does
"Common variants in the NLRP3 region contribute to Crohn's disease susceptibility. [OMIM:NLR FAMILY,..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Neuritic plaques (SNP x SNP interaction) 8E-8 PubMed
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