rs1761667
badMag 3.5This is a upstream gene variant variant in the CD36 gene.
Key Literature Trait Associations
Early-onset coronary artery disease
A 2025 meta-analysis of 25 studies (n=11,494) found that A-allele carriers of rs1761667 had higher HDL-C levels yet paradoxically showed increased risk for early-onset coronary artery disease (EOCAD). This counterintuitive finding may reflect CD36's dual roles in lipid transport, scavenger receptor function, and foam cell formation in atherosclerosis. The authors noted the associations were most pronounced in Chinese populations, and anti-atherosclerotic effects were observed for other CD36 variants (rs1049673, rs3211956) rather than rs1761667. Specific odds ratio values were reported in forest plots but not abstracted numerically.
Fat Taste Sensitivity
CD36 (fatty acid translocase) acts as a receptor on taste cells detecting long-chain fatty acids — the molecules responsible for the creamy, rich quality of high-fat foods. The rs1761667 A allele reduces CD36 expression, lowering oral fat detection. A/A individuals have a higher threshold for tasting fat and may consume more fat to reach satisfaction. G/G individuals detect fat more readily and may feel satisfied with less. This variant also associates with cardiometabolic risk factors in some populations.
Triglyceride levels
A 2022 systematic review and meta-analysis of 18 studies (n=6,317) found that the A allele at rs1761667 is significantly associated with triglyceride levels in allelic (p<0.001), recessive (p=0.001), and homozygous (p=0.006) genetic models. In Asian subgroup analyses, the A allele was also associated with impaired profiles for total cholesterol, LDL-C, and HDL-C. The underlying mechanism likely involves CD36's role in facilitating fatty acid uptake in peripheral tissues, which influences circulating lipid concentrations. Associations with BMI, waist circumference, and blood pressure were not significant in the overall analysis, and effect sizes were not numerically reported in the abstract.
▶ClinVar annotation
▶Research that mentions this SNP (1)
▶Genetic variation of FTO: rs1421085 T>C, rs8057044 G>A, rs9939609 T>A, and copy number (CNV) in Mexican Mayan school‐aged children with obesity/overweight and with normal weightReviewLizbeth González‐Herrera et al.(2019)· American Journal of Human Biology
A literature review of 70 studies examining single nucleotide polymorphisms (SNPs) associated with obesity in Mexican populations published 2011-2021. The authors identified SNPs with differential behavior in Mexican compared to Caucasian populations, including rs17782313 (MC4R), rs6548238 (TMEM18), rs6265 (BDNF), rs7498665 (SH2B1), and notably rs6232 (PCSK1) associated with early-onset obesity in Mexican youth. The review emphasizes ethnicity-dependent genetic effects on BMI heritability (40-70%) and highlights genes involved in cholesterol metabolism and adipokine signaling pathways.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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