| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
AT | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
GA | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||
|
ATTAT | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | 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 | Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. | 21642682 | 2011 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | Mutation spectrum in HNPCC in the Israeli population. | 18389388 | 2008 |
|||
|
TA | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer. | 23047549 | 2012 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Germ-line msh6 mutations in colorectal cancer families. | 10537275 | 1999 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population. | 18566915 | 2009 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer. | 20487569 | 2010 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. | 22006311 | 2011 |
|||
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
AC | 0.700 | CausalMutation | CLINVAR | Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer. | 9929971 | 1999 |
|||
|
AC | 0.700 | CausalMutation | CLINVAR | No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. | 18301448 | 2008 |
|||
|
C | 0.700 | CausalMutation | CLINVAR |