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: McMichael et al., 2015
DOI: 10.1038/mp.2014.189
Study population description: Australian, Caucasian; 98 CP case and parent trios and 67 duos
Regional classification: Oceania
Sequencing or genotyping methods: Whole exome sequencing
| Variant | Reported allele or genotype | Condition | Condition description | Disease status | Odds ratio | P value |
|---|---|---|---|---|---|---|
| NM_004846:c.214C>G | G allele | CP | NESHIE | Not determined | None | None |
| NM_153186:c.243C>G | G allele | CP | Hemiplegia, epilepsy | Not determined | None | None |
| rs1177392425 | T allele | CP | None | Not determined | None | None |