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: Hou et al., 2016
DOI: 10.1007/s12035-015-9566-7
Study population description: Chinese; 105 CP patients and 114 age-, gender-, and ethnicity-matched healthy controls
Regional classification: East Asia
Sequencing or genotyping methods: Genotyping using TaqMan allelic discrimination assay
| Variant | Reported allele or genotype | Condition | Condition description | Disease status | Odds ratio | P value |
|---|---|---|---|---|---|---|
| rs9651118 | CC genotype | CP | None | Susceptibility | None | 0.00200000 |
| rs9651118 | A allele | CP | None | Susceptibility | None | <0.00100000 |
| rs1799724 | T allele | CP | None | Susceptibility | None | 0.03400000 |
| rs361525 | A allele | CP | None | Susceptibility | None | 0.01000000 |
| rs361525 | AA genotype | CP | None | Susceptibility | None | 0.00700000 |
| rs361525 | GG genotype | CP | TNF-a levels | Severity | None | <0.05000000 |