Source: ALL
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.700 | CausalMutation | CLINVAR | New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene. | 26200674 | 2015 |
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|
G | 0.700 | CausalMutation | CLINVAR | Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome. | 25922419 | 2015 |
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|
A | 0.700 | CausalMutation | CLINVAR | Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human. | 22422768 | 2012 |
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|
G | 0.700 | CausalMutation | CLINVAR | Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human. | 22422768 | 2012 |
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|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
AT | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
TC | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR |