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SLC22A1 in SLC47A1 genotype frequencies and the risk for hypoglycemia events.
| Polymorphism | Genotype | All patients | Patients with hypoglycemia | |||
|---|---|---|---|---|---|---|
| N (%) | MAF | N (%) | P | OR (95% CI) | ||
|
SLC47A1
rs2289669 |
GG | 54 (40.3) | 0.355* | 10 (18.5) | 0.310 | 1.38 (0.74–2.59) |
| GA | 65 (48.5) | 13 (20.0) | ||||
| AA | 15 (11.2) | 5 (33.3) | ||||
|
| ||||||
|
SLC22A1
rs628031 |
GG | 51 (37.8) | 0.385 | 15 (29.4) | 0.046 | 0.51 (0.26–0.99) |
| GA | 64 (47.4) | 11 (17.2) | ||||
| AA | 20 (14.8) | 2 (10.0) | ||||
*Data missing for 1 patient; MAF: minor allele frequency.
