[Meta-analysis for the association of GJB2 gene p.V37I variant and its types with the risk of deafness].

Zaihua Wang, Ying Shao, Jun Li

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics（2022）

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摘要

The homozygous c.109G>A (p.V37I) variants of the GJB2 gene and its compound deletional mutation with another GJB2 allele can significantly increase the risk of deafness. Heterozygous c.109G>A (p.V37I) variant of the GJB2 gene or its compound with a missense mutation of another GJB2 allele do not increase the risk.

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关键词

deafness,gene,[meta-analysis

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