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: Jin et al., 2020
DOI: 10.1038/s41588-020-0695-1
Study population description: European, Indian, Mexican, East Asian; 159 CP cases (132 idiopathic, 24 environmental and 3 unclassified) and their unaffected parents were recruited via Phoenix Children’s Hospital (PCH), the University of Adelaide and Zhengzhou City Children’s Hospital.
Regional classification: Europe, America, East Asia, South Asia
Sequencing or genotyping methods: Whole exome sequencing
| Variant | Reported allele or genotype | Condition | Condition description | Disease status | Odds ratio | P value |
|---|---|---|---|---|---|---|
| NM_022002.2:c.1172-1G>T | T allele | CP | None | Not determined | None | None |