rs11873439, CCDC102B

N. diseases: 2
Disease: Myopia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myopia
CUI: C0027092
Disease: Myopia
0.010 GeneticVariation BEFREE Our two-stage genome-wide association study of myopic maculopathy identifies a susceptibility locus at rs11873439 in an intron of CCDC102B (P = 1.77 × 10<sup>-12</sup> and P<sub>corr</sub> = 1.61 × 10<sup>-10</sup>). 29725004 2018