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ABCA1 and myocardial infarction are reported together in 1 article.
Gene
ABCA1
- HGNC
- HGNC:29
21articles
21mentions
5variants with confirmed gene link
Most co-reported phenotypes (articles)
diabetes mellitus 7dyslipidemia 5coronary artery disease 4Alzheimer disease 2obesity 2familial hypercholesterolemia 1hypertension 1metabolic syndrome 1
Reported variants (articles · ClinVar status)
Phenotype
Myocardial infarction
274articles
274mentions
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 60The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians.
PMID 26936456 | PMCID PMC4776394 | DOI 10.1186/s40246-016-0065-3 · Human genomics · 2016 · 10 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ABCA1 | “The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians.” | 0.98 | hgnc_dict_v1 |
| phenotype | myocardial infarction | “Functionally relevant mutations in the dyslipidemia-related genes and enzymes involved in the reverse cholesterol transport system are associated with CAD and contribute to increased susceptibility of myocardial infarction (MI).” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | CETP | “The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians.” | 0.98 | hgnc_dict_v1 |
| phenotype | coronary artery disease | “The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians.” | 0.98 | phenotype_alias_lexicon_v2 |