Source: CLINVAR ×
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
T | 0.700 | CausalMutation | CLINVAR | Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. | 25559809 | 2015 |
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|
T | 0.700 | CausalMutation | CLINVAR | Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer. | 23047549 | 2012 |