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2 records shown · first 60Role of single nucleotide polymorphism rs2383206 on coronary artery disease risk among Saudi Population: a case-control study.
PMID 37522678 | DOI 10.26355/eurrev_202307_33137 · European review for medical and pharmacological sciences · 2023 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs2383206 | “Role of single nucleotide polymorphism rs2383206 on coronary artery disease risk among Saudi Population: a case-control study.” | 0.90 | hgvs_regex_v1 |
| phenotype | coronary artery disease | “Role of single nucleotide polymorphism rs2383206 on coronary artery disease risk among Saudi Population: a case-control study.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | dyslipidemia | “Additionally, individuals with the GG genotype who had sedentary lifestyles, hyperlipidemia, and smoked were found to be at a higher risk for developing CAD (p = 0.003, 0.009, and 0.003, respectively).” | 0.93 | phenotype_alias_lexicon_v2 |
| population | Saudi Arabia | “Role of single nucleotide polymorphism rs2383206 on coronary artery disease risk among Saudi Population: a case-control study. Specifically, the study explores the association between the rs2383206 gene located on chromosome 9p21.3 and the development of coronary artery disease (CAD) in a specific Saudi population. PATIENTS AND METHODS: This case-control study was conducted between September 2013 and May 2015 at King Abdullah Medical City (KAMC) and Al-Noor Specialist Hospital targeting the Saudi Population residing in the western region of Saudi Arabia. The study enrolled 315 cases with documented CAD and 205 controls with normal coronary arteries on coronary angiography.” | 0.95 | saudi_context_rules_v1 |
Coronary Artery Disease: Association Study of 5 Loci with Angiographic Indices of Disease Severity.
PMID 34336004 | PMCID PMC8292076 | DOI 10.1155/2021/5522539 · Disease markers · 2021 · 9 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs2383206 | “Genotyping of five SNPs (namely, rs2230806 (1051G > A) in ABCA1 on chromosome 9, rs2075291 (553G > T) in ApoA5 on chromosome 11, rs320 in LPL on chromosome 8 intron (T → G at position 481), rs10757278 (c.22114477A > G), and rs2383206 (c.22115026 A > G) on chromosome 9p21 locus) was performed by allele-specific PCR.” | 0.90 | hgvs_regex_v1 |
| gene | ABCA1 | “Genotyping of five SNPs (namely, rs2230806 (1051G > A) in ABCA1 on chromosome 9, rs2075291 (553G > T) in ApoA5 on chromosome 11, rs320 in LPL on chromosome 8 intron (T → G at position 481), rs10757278 (c.22114477A > G), and rs2383206 (c.22115026 A > G) on chromosome 9p21 locus) was performed by allele-specific PCR.” | 0.98 | hgnc_dict_v1 |
| gene | LPL | “Genotyping of five SNPs (namely, rs2230806 (1051G > A) in ABCA1 on chromosome 9, rs2075291 (553G > T) in ApoA5 on chromosome 11, rs320 in LPL on chromosome 8 intron (T → G at position 481), rs10757278 (c.22114477A > G), and rs2383206 (c.22115026 A > G) on chromosome 9p21 locus) was performed by allele-specific PCR.” | 0.98 | hgnc_dict_v1 |
| phenotype | coronary artery disease | “Coronary Artery Disease: Association Study of 5 Loci with Angiographic Indices of Disease Severity.” | 0.98 | phenotype_alias_lexicon_v2 |