Variant: rs11866328

present in Gene: GRIN2A present in Chromosome: 16 Position on Chromosome: 9768699 Alleles of this Variant: G/T

rs11866328 in GRIN2A gene and Hepatitis B PMID 22004137 2011 Of the 8 SNPs, variant rs11866328 (G/T), located in the glutamate receptor ionotropic N-methyl D-aspartate 2A (GRIN2A) gene, was replicated and had significant associations with disease progression of HBV infection in the DNA pooling stage both in the Hubei (OR 1.65; 95% CI 1.34,2.02; p=1.96 × 10(-6); additive model), and in the Shandong (OR 1.73; 95% CI 1.14,2.65; p=1.00×10(-2); additive model) population.

rs11866328 in GRIN2A gene and Liver carcinoma PMID 23242368 2013 Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma.