RS10419226 Unknown gene

Other Chr 19:18692362
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What This Variant Does
"rs10419226 is a variant on 19p13 associated with esophageal adenocarcinoma and Barrett&#8217
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) A OR: 1.18 4E-10 PubMed
Barrett's esophagus A OR: 1.19 6E-8 PubMed
Esophageal adenocarcinoma A OR: 1.19 8E-7 PubMed
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