RS77743549 Unknown gene

Other Chr 7:30752287
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What This Variant Does
"Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease"
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Behenoyl dihydrosphingomyelin (d18:0/22:0) levels 2E-6 PubMed
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