Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607008
rs267607008
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		0.700 GeneticVariation UNIPROT The spectrum of WRN mutations in Werner syndrome patients. 16673358

2006