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: Parobek et al., 2024
DOI: 10.1111/cge.14522
Study population description: America; 24 retrospective HIE cases from the Baylor Genetics and Texas Children's Hospital databases
Regional classification: America
Sequencing or genotyping methods: Whole exome sequencing (n=23), whole genome sequencing (n=1)
| Variant | Reported allele or genotype | Condition | Condition description | Disease status | Odds ratio | P value |
|---|---|---|---|---|---|---|
| rs672601369 | T allele | NESHIE | None | Not determined | None | None |
| rs552094593 | A allele | NESHIE | None | Not determined | None | None |
| rs1659975786 | T allele | NESHIE | None | Not determined | None | None |
| NM_014080.4:c.3616G>A | T allele | NESHIE | None | Not determined | None | None |
| rs181461079 | A allele | NESHIE | None | Not determined | None | None |
| rs397507545 | A allele | NESHIE | None | Not determined | None | None |