| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
AG | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||
|
CGGCCTGGAGCGAGGCTG | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. | 25980754 | 2015 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients. | 17909073 | 2007 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Risks of Lynch syndrome cancers for MSH6 mutation carriers. | 20028993 | 2010 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. | 16885385 | 2006 |
|||
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population. | 25318681 | 2015 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Recent progress in Lynch syndrome and other familial colorectal cancer syndromes. | 29485237 | 2018 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Risks of Lynch syndrome cancers for MSH6 mutation carriers. | 20028993 | 2010 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study. | 28125075 | 2017 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. | 25980754 | 2015 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer. | 28135145 | 2017 |
|||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
TG | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
AT | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
AT | 0.700 | CausalMutation | CLINVAR | Risks of Lynch syndrome cancers for MSH6 mutation carriers. | 20028993 | 2010 |