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ALDH3A2 and Alzheimer disease are reported together in 1 article.
Gene
ALDH3A2
- HGNC
- HGNC:403
5articles
5mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype
Alzheimer disease
455articles
455mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease.
PMID 37162726 | PMCID PMC10348954 | DOI 10.1007/s11011-023-01221-7 · Metabolic brain disease · 2023 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ALDH3A2 | “The variants in the ALDH3A2 and RAD54B genes were pathogenic, while in 15 other genes were predicted to be variants of unknown significance.” | 0.98 | hgnc_dict_v1 |
| phenotype | Alzheimer disease | “Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | RAD54B | “The variants in the ALDH3A2 and RAD54B genes were pathogenic, while in 15 other genes were predicted to be variants of unknown significance.” | 0.98 | hgnc_dict_v1 |
| phenotype | intellectual disability | “The disease progresses through several changes, including memory loss, behavioural issues, and cognitive impairment.” | 0.93 | phenotype_alias_lexicon_v2 |