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Phenotype
Leukemia
652articles
652mentions
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 60Association of genetic predisposition studies in CYP1A1 polymorphism studies in acute myeloid leukemia.
PMID 38283773 | PMCID PMC10821586 | DOI 10.1016/j.sjbs.2023.103917 · Saudi journal of biological sciences · 2024 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | leukemia | “Association of genetic predisposition studies in CYP1A1 polymorphism studies in acute myeloid leukemia.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | A4889G | “The aim of this study is to explore the role of A4889G polymorphism in CYP1A1 gene in acute myeloid leukemia (AML) in the Saudi population.” | 0.82 | literature_variant_regex_v2 |
| gene | CYP1A1 | “Association of genetic predisposition studies in CYP1A1 polymorphism studies in acute myeloid leukemia.” | 0.98 | hgnc_dict_v1 |
| population | Saudi Arabia | “The aim of this study is to explore the role of A4889G polymorphism in CYP1A1 gene in acute myeloid leukemia (AML) in the Saudi population. This study was designed as an experimental case-control study in which 100 AML cases and 100 controls were selected. In conclusion, we confirm that A4889G polymorphism is associated with AML in the Saudi population.” | 0.95 | saudi_context_rules_v1 |