RS7005606 Unknown gene

Other Chr 8:32543983
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What This Variant Does
"Variation at NRG1 genotype related to modulation of small-world properties of the functional cortical network."
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Hirschsprung disease G OR: 2.12 1E-11 PubMed
Urate levels T β: 0.021 1E-10 PubMed
Hirschsprung disease — — 3E-7 PubMed
Ask Dr. Hemsworth about this variant