Table 2 also lists three genetic loci at chromosome 2p13.1 (SEMA4F), 2p21 (SPTBN1) and 5q11.1 (PARP8) exhibiting suggestive evidence of association with AL that were seen in at least one SNP with P-values<1×10−5. The gene discussed is SPTBN1; the disease is axial length measurement.