Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554526707
rs1554526707
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		TA 0.700 CausalMutation CLINVAR

dbSNP: rs1554527775
rs1554527775
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1554528411
rs1554528411
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1563331288
rs1563331288
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1563338837
rs1563338837
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1563338855
rs1563338855
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1563341296
rs1563341296
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: rs1563357741
rs1563357741
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1563376347
rs1563376347
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1563376526
rs1563376526
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1563376793
rs1563376793
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		C 0.700 GeneticVariation CLINVAR The spectrum of WRN mutations in Werner syndrome patients. 16673358

2006
dbSNP: rs1563382597
rs1563382597
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1563385391
rs1563385391
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs17847577
rs17847577
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR Clinical utility gene card for: Werner Syndrome--Update 2014. 25182132

2015
dbSNP: rs17847577
rs17847577
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture. 25390333

2014
dbSNP: rs17847577
rs17847577
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR The spectrum of WRN mutations in Werner syndrome patients. 16673358

2006
dbSNP: rs17847577
rs17847577
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR Werner syndrome and mutations of the WRN and LMNA genes in France. 16786514

2006
dbSNP: rs17847577
rs17847577
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: rs17847577
rs17847577
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR Homozygous and compound heterozygous mutations at the Werner syndrome locus. 8968742

1996
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
dbSNP: rs281865157
rs281865157
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs281865158
rs281865158
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		CT 0.700 CausalMutation CLINVAR

dbSNP: rs281865159
rs281865159
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs281865160
rs281865160
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs369158322
rs369158322
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		T 0.700 CausalMutation CLINVAR