A 1.1 kb deletion on chromosome 1 (dbVar ID: nssv15849193, 1:234318630–234,319,762) that disrupts the thiamine transporter SLC35F3 (Solute Carrier Family 35 Member F3) was associated with higher LDL cholesterol in childhood, suggesting the link between thiamine deficiency and dyslipidemia (supplementary figure S7). The gene discussed is SLC35F3; the disease is Thiamine deficiency.