Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11545664
rs11545664
ENG
CUI: C0158570
Disease: Vascular anomaly
Vascular anomaly
0.010 GeneticVariation BEFREE There were no significant associations between ENG c.207G>A and any VM phenotype. 25847705

2015