Additional file 3 of Clinical exome sequencing facilitates the understanding of genetic heterogeneity in Leber congenital amaurosis patients with variable phenotype in southern India

Additional file 3: Supplementary Table S3. Overview of exclusion and prioritization of variants to obtain pathogenic variant from clinical exome data.附加文件3：补充表S3。 从临床外显子组数据中获取致病变异的变异体排除与优先级排序概述。