rs77375493, INSL6;JAK2

N. diseases: 187
Disease: Retinal Vein Occlusion ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Retinal Vein Occlusion
CUI: C0035328
Disease: Retinal Vein Occlusion
0.010 GeneticVariation BEFREE Conventional diagnostic criteria for myeloproliferative disorders and the JAK2 V617F mutation (which is strongly associated with myeloproliferative disorders) were assessed in RVO patients showing EECs. 18054634 2007