HERC2 and OCA2 genes polimorphisms in relation to the iris color variation of the Belarusian population

M. Shapturenko, A. Kondratiuk, S. Vakula, M. V. Seredenko, I. G. Gudzievskaya, S. Borovko, L. N. Marchenko, O. Skrypnik, A. A. Dalidovitch, A. Kilchevsky
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Abstract

The human genetic phenotyping is one of the most intensely developing area of forensic genetics. Externally visible traits, including eye color, can be predicted by analyzing single nucleotide polymorphisms with a high predictive rate. We studied the polymorphisms rs12913832 and rs1800407 in the HERC2 and OCA2 genes, respectively, to evaluate its prognostic availability in relation to the iris pigmentation of the Belarusian population. For this, both eye images and DNA samples were collected from 314 individuals to analyze the key polymorphisms by the TaqMan assay. Our data confirmed a relevance of rs12913832:A>G and rs1800407:G>A in the prediction context. The highest values of the sensitivity (SE = 0.94) and the specificity (SP = 0.90) were obtained for rs12913832, demonstrating the high efficiency of this marker as a classifier of phenotypic groups. The presence of the ancestral dominant allele rs12913832-A causes a dark (brown) iris pigmentation, how- ever, the heterozygous state rs12913832:GA includes a range of mixed variants. The predictive value of rs1800407 for the genetic phenotyping is highly significant (SE = 0.98), but has a low specificity (SP = 0.14), thus rs1800407, not being an effective classifier, can be used as an auxiliary in the eye color predictive model. The analysis of a cumulative impact of the both poly- morphisms on the iris color variation shows their high prospects for the genetic phenotyping of the Belarusian population.
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HERC2和OCA2基因多态性与白俄罗斯人群虹膜颜色变异的关系
人类遗传表型是法医遗传学研究中发展最为活跃的领域之一。外部可见性状,包括眼睛颜色,可以通过分析单核苷酸多态性预测,具有很高的预测率。我们分别研究了HERC2和OCA2基因中rs12913832和rs1800407的多态性,以评估其与白俄罗斯人群虹膜色素沉着的预后可用性。为此,从314个个体中收集眼睛图像和DNA样本,通过TaqMan测定分析关键多态性。我们的数据证实了rs12913832: a >G和rs1800407:G> a在预测上下文中的相关性。rs12913832的敏感性(SE = 0.94)和特异性(SP = 0.90)最高,表明该标记作为表型组的分类器具有较高的效率。祖先显性等位基因rs12913832- a的存在导致虹膜色素沉着,然而,杂合状态rs12913832:GA包括一系列混合变体。rs1800407对遗传表型的预测价值非常显著(SE = 0.98),但特异性较低(SP = 0.14),因此rs1800407不是有效的分类器,可以作为眼颜色预测模型的辅助。对这两种多态性对虹膜颜色变异的累积影响的分析表明,它们对白俄罗斯人群的遗传表型具有很高的前景。
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