rs11545664, ENG

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Vascular anomaly
CUI: C0158570
Disease: Vascular anomaly
0.010 GeneticVariation BEFREE There were no significant associations between ENG c.207G>A and any VM phenotype. 25847705 2015