Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs370324188
rs370324188
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs371538747
rs371538747
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs387906337
rs387906337
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		0.700 GeneticVariation UNIPROT The spectrum of WRN mutations in Werner syndrome patients. 16673358

2006
dbSNP: rs587776621
rs587776621
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		GA 0.700 CausalMutation CLINVAR

dbSNP: rs606231162
rs606231162
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs747587698
rs747587698
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		TG 0.700 CausalMutation CLINVAR

dbSNP: rs748860208
rs748860208
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs752830087
rs752830087
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs757808169
rs757808169
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs758988621
rs758988621
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs759972548
rs759972548
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs763089663
rs763089663
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations. 20443122

2010
dbSNP: rs772319506
rs772319506
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 GeneticVariation CLINVAR The spectrum of WRN mutations in Werner syndrome patients. 16673358

2006
dbSNP: rs774765029
rs774765029
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs776785728
rs776785728
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis. 18810497

2008
dbSNP: rs776785728
rs776785728
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population. 9225981

1997
dbSNP: rs776963381
rs776963381
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs777096501
rs777096501
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 GeneticVariation CLINVAR The spectrum of WRN mutations in Werner syndrome patients. 16673358

2006
dbSNP: rs778872619
rs778872619
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs778872619
rs778872619
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		TA 0.700 CausalMutation CLINVAR

dbSNP: rs780555196
rs780555196
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs797045118
rs797045118
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs878854131
rs878854131
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 GeneticVariation CLINVAR Werner syndrome and mutations of the WRN and LMNA genes in France. 16786514

2006
dbSNP: rs878854131
rs878854131
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 CausalMutation CLINVAR Werner syndrome and mutations of the WRN and LMNA genes in France. 16786514

2006
dbSNP: rs878854133
rs878854133
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 CausalMutation CLINVAR