Table 1.
Gene/SNP ID | Allele/genotype | Subjects | Chromosome region | Genotype frequency | CHB population frequency∗ |
---|---|---|---|---|---|
GRIN1 | 9q34.3 | ||||
rs4880213 | CC/CT/TT | 124/368/340 | 0.15/0.44/0.41 | 0.11/0.44/0.45 | |
rs11146020 | CC/CG/GG | 565/239/28 | 0.68/0.29/0.03 | 0.72/0.24/0.04 | |
GRIN2B | 12p12 | ||||
rs7301328 | CC/CG/GG | 250/396/186 | 0.30/0.48/0.22 | 0.26/0.43/0.31 | |
rs1806201 | AA/AG/GG | 223/438/171 | 0.27/0.53/0.20 | 0.22/0.55/0.22 | |
rs1805247 | AA/AG/GG | 608/204/20 | 0.73/0.25/0.02 | 0.61/0.35/0.04 | |
rs1805502 | AA/AG/GG | 608/203/20 | 0.73/0.24/0.03 | 0.61/0.35/0.04 | |
rs3764028 | AA/AC/CC | 148/397/287 | 0.18/0.48/0.34 | 0.13/0.46/0.42 | |
GRIN2C | 17q25 | ||||
rs3744215 | AA/AC/CC | 143/423/266 | 0.17/0.51/0.32 | 0.15/0.47/0.38 |
∗Data from 1000 Genomes Project Phase 3; http://www.1000genomes.org/.