RETRACTED ARTICLE: The BRCA2 variant c.68-7 T>A is associated with breast cancer
Background BRCA2 c.68-7T>A has been demonstrated to cause aberrant splicing and is possibly pathogenic. The population prevalence of the variant is 0.2%, which higher than usual for pathogenic BRCA2 variants. The pathogenicity of the variant is discussed. Methods The outpatient genetic clinic at...
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Published in | Hereditary cancer in clinical practice Vol. 15; no. 1; pp. 1 - 5 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
13.11.2017
BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1897-4287 1731-2302 1897-4287 |
DOI | 10.1186/s13053-017-0080-y |
Cover
Summary: | Background
BRCA2 c.68-7T>A
has been demonstrated to cause aberrant splicing and is possibly pathogenic. The population prevalence of the variant is 0.2%, which higher than usual for pathogenic
BRCA2
variants. The pathogenicity of the variant is discussed.
Methods
The outpatient genetic clinic at The Norwegian Radium Hospital, part of Oslo University Hospital, has invited breast cancer kindreds for genetic examinations and prospective follow-up of high risk patients since 1988. We have complete files of all activities and results, and we examined the files for association between
BRCA2
c.68-7T>A and breast cancer.
Results
Seventeen out of 714 (2.4%) breast cancer kindreds sequenced for
BRCA2
carried the variant
BRCA2
c.68-7T>A (
p
< 0.0001 compared to population controls). Segregation analysis was inconclusive (likelihood ratio 0.36) for pathogenicity. Two breast cancers were prospectively observed during 134 observation years (annual incidence rate 1.5% (95% CI 0.15% to 5.4%) and one additional breast cancer was diagnosed at first (prevalence) round.
Conclusion
BRCA2
c.68-7T>A is associated with breast cancer. In the families selected due to aggregation of breast cancer, carriers of the
BRCA2
c.68-7T>A variant have increased risk for breast cancer. It is, however, possible that the variant has lower penetrance than the average pathogenic
BRCA2
variants, and that in the families selected for having known aggregation of breast cancer other (modifying) factors contributed to the observed results. |
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ISSN: | 1897-4287 1731-2302 1897-4287 |
DOI: | 10.1186/s13053-017-0080-y |