The Study Findings table contains information on the genetic findings of a particular NESHIE or CP genetic study. Variants with statistically-significant associations with NESHIE or CP have p-values < 0.05. Odds ratio values quantify the strength of association of a variant allele with NESHIE or CP.
Paper: Mei et al., 2021
DOI: 10.1016/j.jpeds.2021.11.019
Study population description: Not stated; 217 patients with CP recruited from Children's Hospital of Fudan University
Regional classification: Not specified
Sequencing or genotyping methods: Clinical exome sequencing of 83 patients (11 trios and 72 singletons) and whole exome sequencing of 134 patients (133 trios and 1 singleton)
| Variant | Reported allele or genotype | Condition | Condition description | Disease status | Odds ratio | P value |
|---|---|---|---|---|---|---|
| rs118192203 | A allele | CP | None | Not determined | None | None |
| rs772800738 | A allele | CP | None | Not determined | None | None |
| rs587777219 | A allele | CP | None | Not determined | None | None |
| NM_003159.3:c.1730_1731dupTG | ATG allele | CP | None | Not determined | None | None |
| rs181461079 | A allele | CP | None | Not determined | None | None |
| NM_172107.4:c.1527delA | C allele | CP | None | Not determined | None | None |
| NM_172107.4:c.172C>A | T allele | CP | None | Not determined | None | None |
| NM_172107.4:c.2326delC | - | CP | None | Not determined | None | None |
| NM_001165963.4:c.4529C>T | A allele | CP | None | Not determined | None | None |
| NM_001165963.4:c.4112G>A | T allele | CP | None | Not determined | None | None |