Table.
Chromo some number |
rs_number | Gene | SNP position within the gene |
Risk allele |
Risk allele frequency |
OR | 95% CI | P-value | |
---|---|---|---|---|---|---|---|---|---|
Cases/Controls | |||||||||
3 | rs1801282 | PPARg | P12A | C | 0.89 | 0.94 | 1.93 | 1.16–3.34 | 0.015 |
3 | rs3856806 | PPARg | H477H | T | 0.16 | 0.14 | 1.13 | 0.77–1.67 | 0.962 |
6 | rs7754840 | CDKAL1 | Intron 5 | C | 0.32 | 0.39 | 1.30 | 1.02–1.88 | 0.038 |
8 | rs13266634 | SCL30A8 | Exon R276W |
C | 0.57 | 0.64 | 1.31 | 0.96–1.72 | 0.091 |
9 | rs10811661 | CDKN2 A/B |
3’-flanking region |
T | 0.67 | 0.68 | 1.04 | 0.74–1.38 | 0.940 |
10 | rs1111875 | HHEX | 3’-flanking region |
C | 0.32 | 0.32 | 1.00 | 0.77–1.39 | 0.820 |
10 | rs7903146 | TCF7L2 | Intron 2 | C | 0.94 | 0.93 | 1.17 | 0.68–2.08 | 0.488 |
11 | rs231361 | KCNQ1 | Intron 11 | G | 0.31 | 0.34 | 1.15 | 0.86–1.54 | 0.348 |
11 | rs2237892 | KCNQ1 | Intron 15 | C | 0.63 | 0.73 | 1.69 | 1.21–2.32 | 0.0020 |
11 | rs2237895 | KCNQ1 | Intron 15 | C | 0.29 | 0.34 | 1.70 | 1.22–2.38 | 0.0020 |
11 | rs2237897 | KCNQ1 | Intron 15 | C | 0.52 | 0.67 | 1.92 | 1.41–2.59 | 3.4×10−5 |
11 | rs5215 | KCNJ11 | Exon 1 V337I |
T | 0.66 | 0.68 | 1.06 | 0.79–1.42 | 0.714 |
11 | rs5219 | KCNJ11 | Exon 1 K23E |
C | 0.67 | 0.68 | 1.07 | 0.80–1.44 | 0.645 |
11 | rs757110 | ABCC8 | Exon 33 A1369S |
A | 0.66 | 0.68 | 1.09 | 0.81–1.46 | 0.577 |
11 | rs1799859 | ABCC8 | Exon 31 R1273R |
G | 0.67 | 0.72 | 1.35 | 0.99–1.84 | 0.057 |
11 | rs2074311 | ABCC8 | Intron 29 | G | 0.68 | 0.69 | 1.03 | 0.77–1.39 | 0.827 |
11 | rs1799854 | ABCC8 | Exon 16 | G | 0.56 | 0.51 | 1.22 | 0.92–1.62 | 0.179 |
11 | rs1799858 | ABCC8 | Exon 14 K649K |
T | 0.16 | 0.23 | 1.78 | 1.23–2.58 | 0.0022 |
11 | rs2074308 | ABCC8 | Intron 11 | T | 0.22 | 0.33 | 1.79 | 1.29–2.50 | 5×10−4 |
11 | rs2237982 | ABCC8 | Intron 10 | C | 0.79 | 0.85 | 1.54 | 1.07–2.24 | 0.023 |
11 | rs1048099 | ABCC8 | Exon 2 P69P |
A | 0.65 | 0.69 | 1.16 | 0.87–1.56 | 0.301 |