Related Experiment Video
Updated: Mar 24, 2026

Inducement and Evaluation of a Murine Model of Experimental Myopia
Published on: January 22, 2019
SNTB1 gene polymorphisms and risk of high myopia: meta-analysis and single-center validation
Jie Peng1, Yina Wang2, Jiaqing Lu2
1Wuxi Huishan District People's Hospital, Wuxi, China.
Purpose:
Genetic polymorphisms in syntrophin beta-1 (SNTB1) have been implicated in altering protein function or expression, potentially influencing ocular growth regulation. Genome-wide association studies (GWASs) suggest that specific SNTB1 variants may correlate with high myopia susceptibility across diverse populations. However, findings remain inconsistent, highlighting the need for further investigation into population-specific genetic effects and underlying mechanisms.
Methods:
Accordingly, the PubMed and Wanfang databases were searched for articles published until June 1, 2025, using the keywords SNTB1 or syntrophin beta-1, polymorphism, and myopia or shortsightedness. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to examine the association. The SNTB1 rs6469937 polymorphism genotypes were identified with the TaqMan assay.
Results:
Four related studies were conducted to better understand the association between SNTB1 gene polymorphisms and high myopia risk. The SNTB1 rs4455882 site was associated with a decreased overall high myopia risk (e.g., G vs. A; OR = 0.815; 95% CI, 0.688-0.984; p heterogeneity = 0.465; p = 0.017). Similar trends were detected in the rs4395927 site (e.g., T vs. C; OR = 0.791; 95% CI, 0.670-0.935; p heterogeneity = 0.199; p = 0.006) and rs6469937 site (e.g., A vs. G; OR = 0.811; 95% CI, 0.697-0.944; p heterogeneity = 0.030; p = 0.007). Furthermore, high myopia patients carrying the SNTB1 rs6469937 AA+AG genotypes exhibited pronounced increases in serum levels of SNTB1 compared to the GG genotype (p < 0.01) but showed an opposite trend compared to genotype-matched normal controls (p < 0.05).
Conclusions:
The current study suggested that the SNTB1 rs4455882, rs4395927, and rs6469937 polymorphisms may be potential influencing factors of high myopia. Furthermore, the rs6469937 polymorphism may offer value as a candidate variant requiring validation that can aid in the early identification and prognostic evaluation of high myopia.
More Related Videos
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Pharmacogenetics of Drug Transporters: P-Glycoprotein and Solute Carrier Transporters
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Genetic Lingo
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

