Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
TA | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
A | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
G | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
G | 0.700 | GeneticVariation | CLINVAR | The spectrum of WRN mutations in Werner syndrome patients. | 16673358 | 2006 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
A | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
G | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | GeneticVariation | CLINVAR | The spectrum of WRN mutations in Werner syndrome patients. | 16673358 | 2006 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
T | 0.700 | CausalMutation | CLINVAR | Clinical utility gene card for: Werner Syndrome--Update 2014. | 25182132 | 2015 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture. | 25390333 | 2014 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | The spectrum of WRN mutations in Werner syndrome patients. | 16673358 | 2006 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | Werner syndrome and mutations of the WRN and LMNA genes in France. | 16786514 | 2006 |
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|
|
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 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | Homozygous and compound heterozygous mutations at the Werner syndrome locus. | 8968742 | 1996 |
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|
|
0.700 | GeneticVariation | UNIPROT | The spectrum of WRN mutations in Werner syndrome patients. | 16673358 | 2006 |
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|
|
G | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
CT | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
G | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
T | 0.700 | CausalMutation | CLINVAR |