Observational Study
Copyright ©The Author(s) 2024.
World J Clin Cases. Jan 26, 2024; 12(3): 503-516
Published online Jan 26, 2024. doi: 10.12998/wjcc.v12.i3.503
Figure 4
Figure 4 Chromatograph of a part of intron 13 sequence showing the c. 2064+9T>C polymorphism (RS79328837). Clinical significance: Benign allele with MAF: 0.002/10. The allele has no pathogenic effect.