Additional file 1: of Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity

Table S1. BMI observations for proband and brother. Table S2. SLIT2 candidate gene. Table S3. SLIT2 mutation whole exome sequencing results. Table S4. Familial genetic co-segregation analysis by whole exome sequencing. Table S5. Variant filtering based on bioinformatics and interpretation. Table S6. Prediction of effects of SLIT2 mutations using the SIFT server. Table S7. Prediction of effects of SLIT2 mutations using the PolyPhen-2 server. Table S8. Prediction of effects of SLIT2 mutations using the PROVEAN server. Table S9. PhyloP conservation scores for SLIT2. (DOCX 35 kb