Gene: NT5E ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906620
rs387906620
NT5E
0.800 GeneticVariation UNIPROT NT5E mutations that cause human disease are associated with intracellular mistrafficking of NT5E protein. 24887587

2014
dbSNP: rs387906620
rs387906620
NT5E
0.800 GeneticVariation UNIPROT NT5E mutations and arterial calcifications. 21288095

2011